Actively Recruiting

Phase 4
Age: 18Years +
FEMALE
NCT07401134

Improving Postoperative Recovery: A Study of Multimodal Perineal Analgesia Protocol (MPAP) After Vaginal Surgery

Led by University of Miami · Updated on 2026-03-04

70

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this research is to determine if using perineal ice packs, medicated witch-hazel pads (MAJOR® Medi-Pads), and topical benzocaine spray (Dermoplast®) helps reduce perineal pain after perineorrhaphy and/or posterior colporrhaphy surgery.

CONDITIONS

Official Title

Improving Postoperative Recovery: A Study of Multimodal Perineal Analgesia Protocol (MPAP) After Vaginal Surgery

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women  18 years of age
  • Undergoing perineorrhaphy and/or posterior colporrhaphy as part of planned vaginal pelvic reconstructive surgery
  • Physically able to apply medicated witch-hazel pads and use topical benzocaine spray on the perineal area
  • Able to understand and willing to provide informed consent
Not Eligible

You will not qualify if you...

  • Allergy or sensitivity to any study products, including witch hazel, benzocaine, aloe, or other ingredients
  • Minors
  • Indwelling catheter expected to remain for 7 or more days after surgery
  • History of chronic pelvic pain syndromes that could affect pain assessment, such as interstitial cystitis, endometriosis, pudendal neuralgia, or vulvodynia
  • Chronic use of opioid pain medication for more than 3 weeks continuously
  • Presence of vulvar skin conditions like lichen sclerosus, lichen planus, or lichen simplex chronicus
  • Currently pregnant or breastfeeding
  • Expected inability to complete postoperative follow-up due to physical or cognitive limitations
  • Unable or unwilling to provide informed consent or follow study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami Hospitals and Clinics

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

K

Katherine Amin, MD

CONTACT

T

Tamar Yacoel, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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