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Study Procedure (all participants) for Premenstrual Dysphoric Disorder (PHASE Project Trial)

N/A
Waitlist Available
Led By Ajna Hamidovic, PharmD, MS
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 hours
Awards & highlights

PHASE Project Trial Summary

This trial is designed to see if a certain medication can help with the symptoms of premenstrual syndrome.

PHASE Project Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one menstrual cycle
This trial's timeline: 3 weeks for screening, Varies for treatment, and one menstrual cycle for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Affect
Cardiovascular function
Estradiol concentrations at 6 menstrual cycle sub-phases
+1 more

PHASE Project Trial Design

1Treatment groups
Experimental Treatment
Group I: Study Procedure (all participants)Experimental Treatment1 Intervention
Diagnostic Phase (2 months): at-home urine hormone testing and completion of daily online surveys. Individualized Task (-6 to -2 days from the subsequent menstrual cycle)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Individualized laboratory test
2019
N/A
~210

Find a Location

Who is running the clinical trial?

University of Illinois at ChicagoLead Sponsor
608 Previous Clinical Trials
1,559,298 Total Patients Enrolled
Ajna Hamidovic, PharmD, MSPrincipal Investigator - University of Illinois at Chicago
University of Illinois at Chicago
1 Previous Clinical Trials
4 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the cap on participant numbers for this clinical trial?

"Affirmative. The data hosted on clinicaltrials.gov indicates that this medical trial, which was first published in September 2019, is currently enrolling patients. One site needs to recruit 120 individuals for the study's completion."

Answered by AI

Does this research endeavor accept participants aged over 25?

"According to the study's requirements, only individuals within the age range of 18-35 are eligible for enrollment."

Answered by AI

May I become a participant in this clinical trial?

"This experiment is searching for 120 females between 18 and 35 years of age who suffer from premenstrual tension. To qualify, individuals must provide documentation that verifies their identity, be within the specified age range mentioned previously, and have a menstrual cycle ranging from 21-35 days in length."

Answered by AI

Are there any openings for participation in this study at the present time?

"Affirmative. On clinicaltrials.gov, it is confirmed that this experiment commenced recruiting on September 26th 2019 and was recently updated as of October 7th 2022. At the moment, 120 patients need to be admitted at one medical centre for the trial to proceed."

Answered by AI
Recent research and studies
~37 spots leftby Apr 2025