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Laparoscopic-Assisted Psoas blockade: A novel post-operative analgesic technique in patients undergoing laparoscopic inguinal hernia repair

A prospective, randomized, clinical trial to evaluate the effect of laparoscopic-assisted psoas blockade versus transversus abdominis plane (TAP) block on post-operative morphine requirements in male patients undergoing laparoscopic inguinal hernia repair

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000632594
Enrollment
45
Registered
2015-06-18
Start date
2015-07-01
Completion date
2016-02-25
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The present study aimed to measure the opioid-sparing effect of the laparoscopic- assisted psoas blockade in comparison with the transversus abdominis plane block in patients undergoing laparoscopic inguinal hernia repair. We hypothesized that the use of laparoscopic- assisted psoas (LAP) blockade can reduce the postoperative analgesic requirements following inguinal herniorraphy.

Interventions

The Laparoscopic-Assisted Psoas blockade was conducted after induction of general anesthesia. Under laparoscopic guidance and after achieving proper exposure of the psoas major muscle, a 5-mm horizontal incision was made in the ventral fascia of the psoas major muscle to provide a proper access for the block catheter. Successful catheter placement was confirmed by expansion of the plane between the psoas muscle and its corresponding fascia with 2 ml normal saline injection. After negative aspir

The Laparoscopic-Assisted Psoas blockade was conducted after induction of general anesthesia. Under laparoscopic guidance and after achieving proper exposure of the psoas major muscle, a 5-mm horizontal incision was made in the ventral fascia of the psoas major muscle to provide a proper access for the block catheter. Successful catheter placement was confirmed by expansion of the plane between the psoas muscle and its corresponding fascia with 2 ml normal saline injection. After negative aspiration, twenty milliliters of plain bupivicaine (2.5 mg/ml) were incrementally administered through the catheter.

Sponsors

Dr tarek Fouad Tammam
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Male patients scheduled for elective laparoscopic unilateral inguinal hernia repair with ASA physical status I–III will be enrolled in the clinical trial.

Exclusion criteria

Patients that had history of allergy to local anesthetics, obesity (BMI 'greater than or equal to' 30 kg/m2), recurrent hernia, neuropathies, or those on chronic analgesic therapies will be excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026