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NCT07251400: analgesia

Analgesic Efficacy of Erector Spinae and Rectus Sheath Block in Patients Undergoing Laparoscopic Inguinal Hernia Repair

Active, enrolled NA Last updated 15 April 2026
What this trial tests

NA trial testing Erector spinae plane block in Erector Spinae Plane Block in 10 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
15 October 2025
Primary endpoint
28 April 2026
30 May 2026

Quick facts

Lead sponsorUmraniye Education and Research Hospital
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment10
Start date15 October 2025
Primary completion28 April 2026
Estimated completion30 May 2026
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Umraniye Education and Research Hospital

Who can join

Adults 18 to 70, any sex, with Erector Spinae Plane Block or Laparoscopic Inguinal Hernia Repair. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study was to compare the effectiveness of ultrasound-guided erector spinae plane block and rectus sheet block on postoperative pain in patients undergoing laparoscopic bilateral hernia repair.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Erector spinae plane block

Trials testing the same drug.

Other recruiting trials for Erector Spinae Plane Block

Currently open trials in the same condition.

Other Umraniye Education and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07251400.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing