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Status unknownNCT00278031Updated Oct 4, 2016

Quality of Life in Children Cured of Retinoblastoma

An observational study in Retinoblastoma, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to participants aged 1 Year to 18 Years. Per ClinicalTrials.gov, last updated 2016-10-04.

Sponsored by Hadassah Medical Organization · Observational

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
35
Ages
1 Year to 18 Years
Sex
All
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Study summary

The aim of the study is to assess the quality of life of children who have been cured of retinoblastoma - a malignant eye tumor. The study is questionnaire-based, and uses standardized quality of life assessment tools.

Read the detailed description

Retinoblastoma is the most common eye tumor of children. It can present in one eye (unilateral) or in both eyes (bilateral). The bilateral form is always hereditary.

Retinoblastoma is a highly curable tumor. Using a combination of surgery, chemotherapy, radiation and local treatment modalities to the eye, over 98% of patients are cured. This means that most children diagnosed with retinoblastoma will become long-term survivors.

The use of surgery (taking out one eye), chemotherapy, and radiation may be associated with long term side-effects, some of which may have significant impact on the quality of life of the child. In addition, in case where the disease is hereditary, additional psychological issues arise.

The aim of our study is to assess, in a comprehensive and standardized fashion, the long term quality of life in children who were treated for retinoblastoma, and who are currently alive and well.

The assessment will include the use of questionnaires that assess quality of life, as well as participation in age-appropriate activities.

Each child, and his/her parent, will be interviewed and the questionnaires completed. The process will take about one hour for each child. No risk or discomfort to the child is involved.

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Conditions studied

  • Retinoblastoma

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Keywords

  • Retinoblastoma
  • Quality of life
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In context

Retinoblastoma

124 studies on the registry are indexed under Retinoblastoma; 23 are open to participants now.

This study's planned enrollment of 35 is below the median of 207 across 36 observational studies indexed under Retinoblastoma.

Browse Retinoblastoma studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 659 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
1 Year to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Long term survivors of childhood retinoblastoma

Eligibility criteria

Inclusion Criteria:

  • Past treatment for retinoblastoma
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
35 participants (estimated)
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What researchers measure

Primary outcomes

  1. Change in quality of life

    Time frame: Baseline and 5 years

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Study locations

1 of 1 sites recruiting
  • Hadassah Medical Organization, Jerusalem, Israel
    Jerusalem, 91120, Israel
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 4, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00278031
Lead sponsor
Hadassah Medical Organization
Collaborators
Israel Cancer Association
Responsible party
Michael Weintraub (DIrector, Pediatric Hematology Oncology, Hadassah Medical Organization) — Principal investigator
First posted
Jan 18, 2006
Start date
Mar 2006
Primary completion
Dec 2017 (estimated)
Completion
Dec 2017 (estimated)
Last update
Oct 4, 2016

Study contacts

Michael Weintraub, MD
Contact
michaelw@hadassah.org.il
972-2-6777408
Michael Weintraub, MD
principal investigator · Hadassah Medical Organization

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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