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Patients receiving transcutaneous suturing for Perineal Pain (PNO Trial)

N/A
Waitlist Available
Led By Lieschen Quiroz, MD
Research Sponsored by University of Oklahoma
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
No Placebo-Only Group

Summary

This trial will compare postoperative perineal pain scores after perineorrhaphy, with either a subcuticular skin closure or interrupted transcutaneous sutures.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Pain level
Secondary study objectives
Patient satisfaction
Perineal pain complications

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Active Control
Group I: Patients receiving transcutaneous suturingActive Control1 Intervention
Sutures will be on your skin
Group II: Patients receiving subcuticular suturingActive Control1 Intervention
Sutures will be hidden underneath skin

Find a Location

Who is running the clinical trial?

University of OklahomaLead Sponsor
473 Previous Clinical Trials
93,579 Total Patients Enrolled
Lieschen Quiroz, MDPrincipal InvestigatorUniversity of Oklahoma HSC
4 Previous Clinical Trials
271 Total Patients Enrolled
~20 spots leftby Nov 2025
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