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The Analgesic Efficacy of Transversus Abdominis Plane Block After Laparoscopic Cholecystectomy

G

Glostrup University Hospital, Copenhagen

Status and phase

Completed
Phase 4

Conditions

Laparoscopic Cholecystectomy

Treatments

Procedure: transversus abdominis plane block
Procedure: TAP block placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01046071
2009-017420-75 (EudraCT Number)
SM1-plp-09

Details and patient eligibility

About

The purpose of this study is to determine whether Transversus abdominis plane block as part of a multimodal postoperative regimen is superior to control in analgesic efficacy after laparoscopic cholecystectomy.

Enrollment

80 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Laparoscopic cholecystectomy
  • ASA 1-3
  • BMI 18-35
  • Written consent

Exclusion criteria

  • Do not understand danish
  • Drug allergy
  • Pregnancy
  • Alcohol or drug abuse
  • Chronic pain with consumption of opioids
  • Consumption of NSAID, COX2inhibitors or paracetamol within 24 hours before the investigation
  • Infection at the needle site.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups, including a placebo group

transversus abdominis plane block
Experimental group
Description:
transversus abdominis plane block with ropivacaine
Treatment:
Procedure: transversus abdominis plane block
block with saline
Placebo Comparator group
Description:
20 ml of isotonic saline bilateral
Treatment:
Procedure: TAP block placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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