NCT07395440

Brief Summary

This study was conducted to evaluate the effectiveness of Quadratus Lumborum Type 1 and Type 2 blocks on postoperative acute pain in gynecological operations performed with a Pfannenstiel incision.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
68

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

April 1, 2025

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

April 19, 2025

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 20, 2025

Completed
25 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2025

Completed
9 months until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
Last Updated

February 9, 2026

Status Verified

February 1, 2026

Enrollment Period

19 days

First QC Date

April 19, 2025

Last Update Submit

February 1, 2026

Conditions

Keywords

quadratus lumborum blockopen gynecological operationsacute pain

Outcome Measures

Primary Outcomes (1)

  • Reduction of opioid requirement in patients undergoing open myomectomy and total abdominal hysterectomy

    It investigates the effectiveness of quadratus lumborum 1 block alone in acute pain, compared to quadratus lumborum 1 and 2 blocks applied together in patients undergoing open myomectomy and total abdominal hysterectomy.

    from april to may

Secondary Outcomes (1)

  • no need for additional analgesia

    from 1 may to 15 may

Eligibility Criteria

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

female patients undergoing open gynecological surgery

You may qualify if:

  • ASA I-III
  • Female patients aged 18-80
  • Cases undergoing open myomectomy and total abdominal hysterectomy

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, Ankara, 06830, Turkey (Türkiye)

Location

Related Publications (3)

  • Koksal E, Aygun H, Genc C, Kaya C, Dost B. Comparison of the analgesic effects of two quadratus lumborum blocks (QLBs), QLB type II vs QLB type III, in caesarean delivery: A randomised study. Int J Clin Pract. 2021 Oct;75(10):e14513. doi: 10.1111/ijcp.14513. Epub 2021 Jun 23.

  • Postoperative analgesic effects of the quadratus lumborum block III and transversalis fascia plane block in paediatric patients with developmental dysplasia of the hip undergoing open reduction surgeries: a double- blinded randomised controlled trial Congcong Huang,1,2 Xiaoguang Zhang,3 Chaoxuan Dong,4 Chunwei Lian Jun Li,2 Lingzhi Yu

    RESULT
  • Bilgin S, Aygun H, Genc C, Dost B, Tulgar S, Kaya C, Sertoz N, Koksal E. Comparison of ultrasound-guided transversalis fascia plane block and anterior quadratus lumborum block in patients undergoing caesarean delivery: a randomized study. BMC Anesthesiol. 2023 Jul 21;23(1):246. doi: 10.1186/s12871-023-02206-w. PMID: 37480008; PMCID: PMC10362577.

    RESULT

MeSH Terms

Conditions

Acute Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • KADİR T ETİKCAN, MEDİCAL DOCTOR

    ANKARA ETLİK CİTY HOSPİTAL

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Specialist

Study Record Dates

First Submitted

April 19, 2025

First Posted

February 9, 2026

Study Start

April 1, 2025

Primary Completion

April 20, 2025

Study Completion

May 15, 2025

Last Updated

February 9, 2026

Record last verified: 2026-02

Locations