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The Addition of Sufentanil Interscalene Block in Shoulder Surgery

B

Bent Gymoese Jorgensen

Status and phase

Completed
Phase 3

Conditions

Postoperative Pain
Shoulder Surgery

Treatments

Drug: Naropin 0.1% cum sufentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT01025102
gymoese007

Details and patient eligibility

About

The purpose of this study is to compare the effects and side effects of interscale block performed with Naropin 0.1% cum sufentanil or Naropin 0.1% in shoulder surgery.

Full description

The purpose of this study is to compare the duration of postoperative analgesia and supplemental opioid consumption and side effects of interscale block performed with Naropin 0.1% cum sufentanil or Naropin 0.1% in shoulder surgery

Enrollment

26 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-III
  • Age 18-80
  • Shoulder surgery performed under interscalene block and general anesthesia

Exclusion criteria

  • Contraindication of interscalene block
  • Severe chronic obstructive lung disease
  • Non-cooperative patient
  • Intolerance to opioids
  • Pregnancy
  • Rheumatoid arthritis and diabetes with peripheral polyneuropathy
  • Chronic pain or daily opioid intake

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

26 participants in 1 patient group

Naropin 0.1%
Experimental group
Treatment:
Drug: Naropin 0.1% cum sufentanil

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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