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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05540392
Other study ID # 22-270
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date September 9, 2022
Est. completion date September 2024

Study information

Verified date October 2023
Source Memorial Sloan Kettering Cancer Center
Contact Kevin Liou, MD
Phone 646-608-8558
Email liouk@mskcc.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test whether acupuncture can improve nocturia in prostate cancer survivors. This is the first time acupuncture is being studied for nocturia in prostate cancer survivors. Researchers will see if acupuncture is a practical treatment option for prostate cancer survivors with nocturia. The study will also look at the effect acupuncture has on nocturia and other symptoms prostate cancer survivors experience such as insomnia, hot flashes, anxiety, depression, tiredness (fatigue), sexual dysfunction, and cognitive (mental) difficulties.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 or older - Prior PC diagnosis - No evidence of Prostate Cancer - Clinically meaningful nocturia, defined as =2 nocturia episodes every night for the past month Exclusion Criteria: - <1 month since completion of PC treatment (surgery, chemotherapy, radiation, ADT) - Score of =5 on the STOP-Bang questionnaire indicative of high risk of moderate-to severe obstructive sleep apnea - Other untreated primary sleep disorder (e.g. delayed/advanced sleep phase syndrome) - Untreated primary psychiatric disorder (e.g. bipolar disorder, schizophrenia, substance abuse, dementia) - Initiation of new medications for urinary symptoms in the past 4 weeks - Altered dosing of medications for urinary symptoms in the past 4 weeks - Plan to initiate/change medications or other treatments (e.g. surgery, behavioral intervention, complementary therapies) for urinary symptoms during the study - Implanted electronically charged medical device - Unable to provide consent for himself - Unwilling to adhere to all study-related procedures

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture
10 treatments of acupuncture over the course of 10 weeks
Other:
Waitlist Control
The waitlist control group will not receive any acupuncture treatments during the 14-week waiting period. Patients in waitlist control group will have the option to receive up to 10 acupuncture treatments after a 14-week waiting period.
Questionnaires
Patients will complete Patient Reported Outcomes (PRO)

Locations

Country Name City State
United States Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey
United States Memorial Sloan Kettering Cancer Center Suffolk - Commack Commack New York
United States Memorial Sloan Kettering Westchester Harrison New York
United States Memorial Sloan Kettering Monmouth Middletown New Jersey
United States Memorial Sloan Kettering Bergen Montvale New Jersey
United States Memorial Sloan Kettering Cancer Center New York New York
United States MSK at Ralph Lauren (Consent Only) New York New York
United States Memorial Sloan Kettering Nassau Uniondale New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary success If a participant completes at least 8 out of 10 acupuncture sessions. Feasibility will be evaluated based on the respective definitions of success for the acupuncture. 1 year
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