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← Ovarian Neoplasm

NCT00550654 · STUDY IN CONTEXT

Conformal Radiation Therapy in Treating Patients With Metastatic Cancer Outside the Brain

Draft scope assessment: narrower. Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. The condition was transformed or resolved through the terminology hierarchy to reach this cancer type, so the link itself is a candidate a reviewer must confirm. Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.

Read the full study record and all posted results →

Linked outcomes

Measures are not ranked. Open each original source section for treatment groups, denominators, units and results.

primary · POSTED

Local control (e.g. absence of local progression) is defined as Complete response (CR), partial response (PR) or stable disease (SD) of the treated site(s). Complete response is the disappearance of the target lesion. Partial response is a \>/= 50% decrease in maximal dimension compared to pretreatment imaging. Stable disease does not qualify for CR, PR, or progression.Progression is an interval increase in the maximal dimension of the target lesion.

No data/specimens were collected. Study was terminated due to poor accrual.

→

secondary · POSTED

Here is the number of participants with adverse events. For the detailed list of adverse events see the adverse event module.

Source null

→

secondary · POSTED

Interval from initiation of treatment on protocol to symptomatic or radiographic progression.

No data/specimens were collected. Study was terminated due to poor accrual.

→

secondary · POSTED

Local control (e.g. absence of local progression) is defined as Complete response (CR), partial response (PR) or stable disease (SD) of the treated site(s). Complete response is the disappearance of the target lesion. Partial response is a \>/= 50% decrease in maximal dimension compared to pretreatment imaging. Stable disease does not qualify for CR, PR, or progression. Progression is an interval increase in the maximal dimension of the target lesion.

No data/specimens were collected. Study was terminated due to poor accrual.

→

secondary · POSTED

Megavoltage localization scans will be obtained and the physician and therapist will evaluate the cone beam image and compare this image to the expected image based on the patient's initial planning CT scan.

No data/specimens were collected. Study was terminated due to poor accrual.

→

secondary · POSTED

Improvement in pain from baseline will be assessed by the Brief Inventory for Pain criteria.

No data/specimens were collected. Study was terminated due to poor accrual.

→

Reported safety

Serious events are not the same as severe events. Compare the original safety groups and their at-risk populations.

Open the study safety table →

Quality of life and patient-reported measures

No linked quality-of-life measure is recorded for this setting and study.

Full draft applicability and source-link record
trial
release id
clinical-indications-draft-1
disease state id
ds-ovarian-neoplasm
nct id
NCT00550654
trial label
Conformal Radiation Therapy in Treating Patients With Metastatic Cancer Outside the Brain
applicability
narrower
applicability note
Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. The condition was transformed or resolved through the terminology hierarchy to reach this cancer type, so the link itself is a candidate a reviewer must confirm.
curation status
draft
reviewed by
Source null
reviewed at
Source null
created at
2026-09-10T00:00:00Z
provenance class
registry-condition-search
discovery note
Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
outcome Count
6
harms Count
1
qol Count
0
outcomes
  1. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0000
    source section id
    NCT00550654-om-0000
    source outcome index
    0
    endpoint
    6-month Local Control (i.e., Complete Response, Partial Response, or Stable Disease) at All Treated Sites of Metastatic Disease
    endpoint definition
    Local control (e.g. absence of local progression) is defined as Complete response (CR), partial response (PR) or stable disease (SD) of the treated site(s). Complete response is the disappearance of the target lesion. Partial response is a \>/= 50% decrease in maximal dimension compared to pretreatment imaging. Stable disease does not qualify for CR, PR, or progression.Progression is an interval increase in the maximal dimension of the target lesion.
    time origin
    6 months
    analysis role
    primary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    No data/specimens were collected. Study was terminated due to poor accrual.
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
  2. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0001
    source section id
    NCT00550654-om-0001
    source outcome index
    1
    endpoint
    Number of Participants With Adverse Events
    endpoint definition
    Here is the number of participants with adverse events. For the detailed list of adverse events see the adverse event module.
    time origin
    9 months, 11 days
    analysis role
    secondary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    Source null
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
  3. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0002
    source section id
    NCT00550654-om-0002
    source outcome index
    2
    endpoint
    Median Time to Local Progression
    endpoint definition
    Interval from initiation of treatment on protocol to symptomatic or radiographic progression.
    time origin
    6-12 months
    analysis role
    secondary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    No data/specimens were collected. Study was terminated due to poor accrual.
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
  4. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0003
    source section id
    NCT00550654-om-0003
    source outcome index
    3
    endpoint
    12 Month Local Control in All Sites of Treatment, and at Each Site of Treatment
    endpoint definition
    Local control (e.g. absence of local progression) is defined as Complete response (CR), partial response (PR) or stable disease (SD) of the treated site(s). Complete response is the disappearance of the target lesion. Partial response is a \>/= 50% decrease in maximal dimension compared to pretreatment imaging. Stable disease does not qualify for CR, PR, or progression. Progression is an interval increase in the maximal dimension of the target lesion.
    time origin
    12 months
    analysis role
    secondary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    No data/specimens were collected. Study was terminated due to poor accrual.
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
  5. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0004
    source section id
    NCT00550654-om-0004
    source outcome index
    4
    endpoint
    Interfraction and Intrafraction Motion With Megavoltage Computed Tomography (CT) Based on Sites of Metastasis
    endpoint definition
    Megavoltage localization scans will be obtained and the physician and therapist will evaluate the cone beam image and compare this image to the expected image based on the patient's initial planning CT scan.
    time origin
    One to three months of followup
    analysis role
    secondary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    No data/specimens were collected. Study was terminated due to poor accrual.
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
  6. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0005
    source section id
    NCT00550654-om-0005
    source outcome index
    5
    endpoint
    Pain at Sites of Metastases
    endpoint definition
    Improvement in pain from baseline will be assessed by the Brief Inventory for Pain criteria.
    time origin
    One and three months of follow up
    analysis role
    secondary
    reporting status
    POSTED
    data cutoff
    Source null
    population note
    No data/specimens were collected. Study was terminated due to poor accrual.
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
arms
  1. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0000
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    0
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0000#groups/OG000
  2. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0001
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    1
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0001#groups/OG000
  3. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0002
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    0
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0002#groups/OG000
  4. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0003
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    0
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0003#groups/OG000
  5. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0004
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    0
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0004#groups/OG000
  6. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    outcome key
    om-0005
    arm key
    OG000
    arm label
    Radiation Therapy in Metastatic Cancer
    regimen
    Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions.
    analyzed count
    0
    analyzed unit
    Participants
    is comparator
    Source null
    source pointer
    NCT00550654-om-0005#groups/OG000
harms
  1. release id
    clinical-indications-draft-1
    disease state id
    ds-ovarian-neoplasm
    nct id
    NCT00550654
    harm key
    EG000
    source section id
    NCT00550654-ae
    event group key
    EG000
    event group label
    Radiation Therapy in Metastatic Cancer
    serious affected
    0
    serious at risk
    1
    other affected
    1
    other at risk
    1
    frequency threshold
    0
    collection period
    Source null
    event definition
    Source null
    undenominated note
    Source null
    curation status
    draft
    reviewed by
    Source null
    reviewed at
    Source null
    created at
    2026-09-10T00:00:00Z
quality of life
    setting source links

      Preserved source evidence · Not medical advice