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The Effect of Pre-Operative Transversus Abdominis Plane (TAP) Block in the Post Operative Opioid Consumption in Morbid Obese Patients Undergoing Laparoscopic Gastric Bypass Surgery: A Prospective,Randomized, Blinded Study

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Northwestern University

Status

Completed

Conditions

Surgery
Obesity
Pain

Treatments

Drug: (study group) will receive a bilateral TAP block using 20 cc of 0.5% ropivacaine on each side.
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01075087
STU00023482

Details and patient eligibility

About

The use of preoperative TAP block in laparoscopic bariatric surgery can improve the postoperative pain and quality of recovery in patients undergoing these procedures.

Enrollment

19 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: 18-65 years
  • BMI >35 Kg/m2
  • Surgery: laparoscopic gastric bypass surgery
  • ASA status: I, II and III
  • Fluent in English

Exclusion criteria

  • History of allergy to local anesthetics
  • Chronic opioid use
  • Pregnant patients
  • Patients who remained intubated after surgery

Drop-out criteria:

Patient or surgeon request Complications related to the procedure or conversion to open route Patient requiring mechanical ventilation after surgery

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

19 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
(control group) will receive sterile normal saline in the block
Treatment:
Drug: Placebo
Active comparator
Active Comparator group
Description:
(study group) will receive a bilateral TAP block using 20 cc of 0.5% ropivacaine on each side.
Treatment:
Drug: (study group) will receive a bilateral TAP block using 20 cc of 0.5% ropivacaine on each side.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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