Amenorrhea Clinical Trials

Find Amenorrhea Clinical Trials Near You

Acupuncture for Adolescent and Young Adult Cancer Patients: (AcuAYA)

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Other, Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The purpose of this study is to find out whether it is practical (feasible) to use acupuncture to treat period loss (amenorrhea) caused by chemotherapy treatment in people with cancer. The researchers will look at how many participants enroll and complete the study. The researchers will also study how treatment with acupuncture affects the amount of time for the menstrual cycle to return and symptoms and quality of life related to amenorrhea.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 15
Maximum Age: 40
Healthy Volunteers: f
View:

• English speaking woman between the ages of 15 and 40

• History of stage I, II, or III cancer OR stage IV or unstaged hematologic malignancy (e.g. lymphoma, leukemia, myeloma) that is stable, as assessed by care team

• Premenopausal status with regular menstruation at the time of diagnosis by patient report

• Completed cytotoxic chemotherapy within the past year

• Premenopausal status with regular menstruation at the time of diagnosis by patient report for females ages 18 or older

• Report cessation of menses during or after chemotherapy and have not experienced menses recovery at the time of enrollment.

• Have reached menarche prior to therapy or during therapy for females between 15 and 17 years old

• Patient reports cessation of menses during or after chemotherapy and have not experienced menses recovery at the time of enrollment.

• Have been without menses for at least 3 months 64 following the completion of cytotoxic chemotherapy

• Willing to adhere to all study-related procedures, including randomization to one of the two possible arms: acupuncture and WLC

Locations
United States
New Jersey
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth (All protocol activities)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (All Protocol Activities)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Suffolk- Commack (All Protocol Activities)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (All Protocol Activities)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
RECRUITING
New York
Memorial Sloan Kettering Nassau (All Protocol Activities)
RECRUITING
Rockville Centre
Contact Information
Primary
Jun Mao, MD, MSCE
maoj@mskcc.org
646-608-8553
Backup
William Tap, MD
646-888-4163
Time Frame
Start Date: 2025-03-31
Estimated Completion Date: 2027-03-31
Participants
Target number of participants: 60
Treatments
Experimental: Acupuncture group
Participants in the acupuncture group will receive 12 acupuncture treatments over 12 weeks during the study.
Active_comparator: Wait-list Control (WLC)
Participants in the wait-list control group will be put on a wait-list and have the option to receive the same acupuncture treatment as the acupuncture group after a 16-week waiting period. The 16-week waiting period will begin on the day that the WLC participant completes their baseline lab draw.
Related Therapeutic Areas
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov