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Effects of Local Anesthesia on Post-operative Pain During Laparoscopic Inguinal Hernia Repair

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Lahey Health

Status and phase

Completed
Phase 4

Conditions

Post Operative Pain (Post Laparoscopic Hernia Repair)

Treatments

Drug: 0.5% Bupivicaine

Study type

Interventional

Funder types

Other

Identifiers

NCT02055053
LCID 2013-031

Details and patient eligibility

About

To assess effect of local anesthetic into the preperitoneal space during laparoscopic hernia repair on post-operative pain.

Enrollment

70 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18 or older with unilateral or bilateral inguinal herna for laparoscopic repair
  • American Society of Anesthesiology (ASA) Class I and II

Exclusion criteria

  • Conversion from laparoscopic to open surgery
  • History of Chronic pain or ongoing treatment for chronic pain
  • Age less than 18 yrs
  • Allergy to local anesthetics

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups, including a placebo group

anesthetic intervention
Experimental group
Description:
After deployment of therapeutic mesh in the preperitoneal space of the abdomen wall during the procedure, the treatment group will receive infusion of 15 cc 0.5% Bupivicaine.
Treatment:
Drug: 0.5% Bupivicaine
Saline intervention
Placebo Comparator group
Description:
After deployment of therapeutic mesh in the preperitoneal space of the abdomen wall during the procedure, the placebo group will receive the infusion of 15 cc 0.9% Saline.
Treatment:
Drug: 0.5% Bupivicaine

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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