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NCT05540392Active, not recruitingPhase 1/2

An Acupuncture Study for Prostate Cancer Survivors With Urinary Issues

Nocturia in Prostate Cancer Survivors - Acupuncture Pilot Study (NOCTURNAL)

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
60 (actual)
First submitted
9 Sept 2022
Start date
9 Sept 2022
Primary completion date
Sept 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT05540392

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 60
  • From 9 Sept 2022 to the primary completion date, Sept 2027
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • \<1 month since completion of PC treatment (surgery, chemotherapy, radiation, ADT)
  • 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

Other illness

  • Other untreated primary sleep disorder (e.g. delayed/advanced sleep phase syndrome)
  • Untreated primary psychiatric disorder (e.g. bipolar disorder, schizophrenia, substance abuse, dementia)

Other

  • Score of ≥5 on the STOP-Bang questionnaire indicative of high risk of moderate-to severe obstructive sleep apnea
  • Implanted electronically charged medical device
  • Unable to provide consent for himself
  • Unwilling to adhere to all study-related procedures

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Basking Ridge
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center @ Suffolk - Commack
Coordinator of this site? Confirm its status
CommackUnited StatesUnknown status
Memorial Sloan Kettering Westchester
Coordinator of this site? Confirm its status
HarrisonUnited StatesUnknown status
Memorial Sloan Kettering Monmouth
Coordinator of this site? Confirm its status
MiddletownUnited StatesUnknown status
Memorial Sloan Kettering Bergen
Coordinator of this site? Confirm its status
MontvaleUnited StatesUnknown status
MSK at Ralph Lauren (Consent Only)
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Memorial Sloan Kettering Nassau
Coordinator of this site? Confirm its status
UniondaleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.