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The Effect of Tramadol on Interscalene Brachial Plexus Block

A

Asklepieion Voulas General Hospital

Status and phase

Completed
Phase 2

Conditions

Shoulder Dislocation
Shoulder Fracture
Shoulder Arthritis
Rotator Cuff Injury

Treatments

Drug: Ropivacaine
Drug: Ropivacaine - Tramadol

Study type

Interventional

Funder types

Other

Identifiers

NCT02182752
3694/27-3-13

Details and patient eligibility

About

The purpose of our study is to evaluate the effect of tramadol as an adjunct to ropivacaine local anesthetic solution in interscalene brachial plexus block for shoulder surgery.

Enrollment

80 patients

Sex

All

Ages

18 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Shoulder surgery

Exclusion criteria

  • patients on opioids
  • diabetes mellitus
  • interscalene block contraindicated
  • patient refusing regional anesthesia techniques

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups

Ropivacaine - Tramadol
Active Comparator group
Treatment:
Drug: Ropivacaine - Tramadol
Ropivacaine
Active Comparator group
Treatment:
Drug: Ropivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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