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NCT00001177 · ClinicalTrials.gov registry record

Study of Premenstrual Syndrome and Premenstrual Dysphoria

A clinical trial of Mood Disorder, sponsored by National Institute of Mental Health (NIMH).

Recruiting
Registry status
1,600
Enrollment target
1
Study location

NCT00001177: Recruiting study of Mood Disorder, sponsored by National Institute of Mental Health (NIMH).

NCT00001177 is a study of Mood Disorder that is actively recruiting participants, run by National Institute of Mental Health (NIMH). The registered enrollment target is 1,600 participants, above the 1,079-participant average among 7 other Mood Disorder trials with a reported enrollment target (48% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00001177, a study of Mood Disorder, is actively recruiting participants, sponsored by National Institute of Mental Health (NIMH).

RECRUITING
Registry status
1,600 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to identify and describe the symptoms of premenstrual syndrome (PMS). Women who experience PMS symptoms will complete clinical interviews, self-rating scales, and evaluations of mood and endocrine function. A subgroup of women with severe PMS (Premenstrual Dysphoric Disorder or PMDD) will be offered additional research studies that focus on: 1) identifying the endocrine changes that may be responsible for changes in mood and behavior during the premenstrual period, 2) evaluating treatments for PMS symptoms, and/or 3) identifying genetic factors in women with and without PMS. Women with recurrent brief depression will also be recruited to serve as a comparison group....

Primary Outcome

Standardized cross-sectional rating scales (Beck Depression Inventory, Hamilton Depression and Anxiety Scales, and the Rating Scale for Premenstrual Tension Syndrome), symptom rating scales completed daily, and plasma hormone measures (including neurosteroid levels).

Conditions Studied

Study Locations (1)

Maryland

  • National Institutes of Health Clinical Center - Bethesda

Trial Details

FieldValue
Enrollment Target 1,600 participants
Start Date 1984-03-09

What NCT00001177 shows while recruiting

NCT00001177 is an observational study that tracks outcomes without assigning an intervention. Its 1,600 participants enrollment target places it among the larger protocols in the corpus, above the 1,079-participant average among 7 other Mood Disorder trials with a reported enrollment target (48% higher).

The record links to 1 condition, with Mood Disorder appearing as the primary indexed condition, and to 0 interventions.

NCT00001177 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT00001177 about?

NCT00001177 is a clinical study titled "Study of Premenstrual Syndrome and Premenstrual Dysphoria". The purpose of this study is to identify and describe the symptoms of premenstrual syndrome (PMS). Women who experience PMS symptoms will complete clinical interviews, self-rating scales, and evaluations of mood and endocrine function. A subgroup of women with severe PMS (Premenstrual Dysphoric Dis...

What is the current status of trial NCT00001177?

This trial is currently recruiting. The enrollment target is 1,600 participants. The study started on 1984-03-09.

What conditions does trial NCT00001177 study?

This clinical trial studies the following conditions: Mood Disorder.

Who is sponsoring clinical trial NCT00001177?

This trial is sponsored by National Institute of Mental Health (NIMH), which has 343 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00001177 being conducted?

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

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Source: ClinicalTrials.gov NCT00001177, the US trial registry maintained by the National Library of Medicine. NCT00001177 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.