NCT07114965

Brief Summary

This study was conducted to evaluate the effectiveness of Quadratus Lumborum Type 1 and Transversalis Fascial Plane blocks on postoperative acute pain in gynecology operations.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
68

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
5 days until next milestone

First Submitted

Initial submission to the registry

July 6, 2025

Completed
26 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

August 11, 2025

Completed
Last Updated

August 11, 2025

Status Verified

August 1, 2025

Enrollment Period

1 month

First QC Date

July 6, 2025

Last Update Submit

August 4, 2025

Conditions

Postoperative PainGynecologic Surgery

Outcome Measures

Primary Outcomes (1)

  • Postoperative pain between groups

    The steps of expanding the transversalis fascial plane in acute pain are being investigated against the quadratus lumborum 1 spread applied in gynecological surgery.

    day 1

Secondary Outcomes (2)

  • Time to first rescue analgesic consumption

    day 1

  • total opioid consumption

    day 1

Study Arms (1)

open gynecological operations

Eligibility Criteria

Age18 Years - 80 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsgynecologic surgery
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Women who have undergone open gynecological surgery

You may qualify if:

  • ASA I-III
  • years old women's medicines
  • Open myomectomy and total abdominal hysterectomy cases

You may not qualify if:

  • Those who do not want a block
  • Patients who are allergic to local anesthetics
  • Patients with coagulopathy ·
  • Pregnancy
  • Previous surgery in the area where the block will be applied

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Etlik City Hospital

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
specialist doctor

Study Record Dates

First Submitted

July 6, 2025

First Posted

August 11, 2025

Study Start

June 1, 2025

Primary Completion

July 1, 2025

Study Completion

August 1, 2025

Last Updated

August 11, 2025

Record last verified: 2025-08

Locations

TU(1)