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Acupuncture for Postoperative Urinary Retention After Hemorrhoidectomy: a Randomized Controlled Trial

C

Chengdu University of Traditional Chinese Medicine

Status and phase

Completed
Phase 2

Conditions

Postoperative Complications
Postoperative Urinary Retention

Treatments

Other: Acupuncture
Other: Sham acupuncture
Drug: Neostigmine Injectable Product

Study type

Interventional

Funder types

Other

Identifiers

NCT05898919
HCDUTCM_2022056

Details and patient eligibility

About

The goal of this study is to examine the efficacy of acupuncture in the management of acute postoperative urinary retention.

Clinical question:

Is acupuncture efficacious for postoperative urinary retention after hemorrhoidectomy compared with sham acupuncture and neostigmine.

Study design:

The participants who undergo hemorrhoidectomy and report postoperative urinary retention will receive one session of acupuncture or sham acupuncture or one injection of 1-mg neostigmine. The primary outcome was the time to first urination after surgery.

Enrollment

92 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged between 18 and 65 years
  • Meets the diagnostic criteria of postoperative urinary retention
  • Received milligan-morgan hemorrhoidectomy and general anesthesia

Exclusion criteria

  • Received Diuretic drugs
  • Organic diseases that cause urinary retention
  • Severe infection in the urinary tract
  • Has a history of adverse reaction to neostigmine
  • Cognitive dysfunction that affects outcome assessment
  • Being pregnant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

92 participants in 3 patient groups, including a placebo group

Acupuncture
Experimental group
Treatment:
Other: Acupuncture
Sham acupuncture
Placebo Comparator group
Treatment:
Other: Sham acupuncture
Neostigmine
Active Comparator group
Treatment:
Drug: Neostigmine Injectable Product

Trial contacts and locations

1

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Central trial contact

Tai-Chun Tang, MD

Data sourced from clinicaltrials.gov

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