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NCT01738152 · ClinicalTrials.gov registry record · NA

Non-Hormonal Vaginal Moisturizer in Hormone-Receptor Positive Postmenopausal Cancer Survivors Experiencing Estrogen Deprivation Symptoms on Vulvovaginal Health

A NA study of Breast Cancer and Endometrial Cancer, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
NA
Development phase
106
Enrollment target
1
Study location

NCT01738152: Completed NA study of Breast Cancer and Endometrial Cancer, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01738152 is a NA study of Breast Cancer and Endometrial Cancer that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 106 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01738152, a NA study of Breast Cancer and Endometrial Cancer, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
NA
Development phase
106 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to see whether it is feasible to conduct a study to determine if the use of hyaluronic acid (HLA) vaginal gel (HyaloGYN®) improves vulvovaginal health. This study aims to look at whether or not HyaloGYN® is effective in women with a history of hormone receptor positive cancer and experiencing vaginal and/or vulvar symptoms of estrogen deprivation following their breast and endometrial cancer treatment.

Primary Outcome

a 12-week HLA treatment regimen, as defined by the percentage of women who are evaluable at the 12-week assessment (i.e., women who have completed both baseline and 12-week vaginal and vulvar outcome assessments).

Interventions

  • BEHAVIORAL questionnaires
  • OTHER HLA vaginal gel (HyaloGYN®),

Study Locations (1)

New York

  • Memorial Sloan Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2012-11
Est. Completion 2021-07-21
Phase NA
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT01738152 record still lists

NCT01738152 is an interventional study that assigns participants to a tested intervention. The registered 106 participants enrollment target is mid-sized for trials with a published cap, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower).

The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which questionnaires is the first listed.

NCT01738152 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT01738152 about?

NCT01738152 is a clinical study titled "Non-Hormonal Vaginal Moisturizer in Hormone-Receptor Positive Postmenopausal Cancer Survivors Experiencing Estrogen Deprivation Symptoms on Vulvovaginal Health". The purpose of this study is to see whether it is feasible to conduct a study to determine if the use of hyaluronic acid (HLA) vaginal gel (HyaloGYN®) improves vulvovaginal health. This study aims to look at whether or not HyaloGYN® is effective in women with a history of hormone receptor positive ...

What is the current status of trial NCT01738152?

This trial is currently completed. It is a NA study. The enrollment target is 106 participants. The study started on 2012-11. Estimated completion is 2021-07-21.

What conditions does trial NCT01738152 study?

This clinical trial studies the following conditions: Breast Cancer, Endometrial Cancer.

What interventions are being tested in trial NCT01738152?

The interventions under investigation include: questionnaires (BEHAVIORAL), HLA vaginal gel (HyaloGYN®), (OTHER).

Who is sponsoring clinical trial NCT01738152?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01738152 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Breast Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01738152's enrollment target sits among peer trials

106 549th of 1224 higher than 676 of 1,224 other Breast Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Breast Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01738152, the US trial registry maintained by the National Library of Medicine. NCT01738152 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.