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Clinical Trials/EUCTR2020-001215-24-DK
EUCTR2020-001215-24-DK
Active, not recruiting
Phase 1

The effect of subpectineal obturator nerve block on opioid consumption and pain after hip arthroscopy A double-blind randomized, controlled trial

Aarhus University Hospital0 sites40 target enrollmentMarch 30, 2020
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ConditionsPostoperative pain after hip arthroscopyMedDRA version: 21.0Level: LLTClassification code 10080604Term: Hip arthroscopySystem Organ Class: 100000004848Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsMarcain-Adrenalin

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Postoperative pain after hip arthroscopy
Sponsor
Aarhus University Hospital
Enrollment
40
Status
Active, not recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 30, 2020
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Aarhus University Hospital

Eligibility Criteria

Inclusion Criteria

  • •Set for elective primary hip arthroscopy by one single orthopedic surgeon
  • •Scheduled general anesthesia with Propofol and Remifentanil
  • •ASA I\-III
  • •Patient \= 18 years
  • •Informed consent
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range 35
  • •F.1\.3 Elderly (\>\=65 years) yes

Exclusion Criteria

  • •Inability to cooperate
  • •Unable to speak and/or understand Danish or other forms of communication problems
  • •Allergy to local analgesics used in the study (Marcain \+ Adrenaline).
  • •Lack of tolerance to both Morphine and Oxycodone
  • •Chronic pain with daily opioid consumption (dosed \> 1day)
  • •Treatment with antipsychotics
  • •Known abuse of alcohol or medication
  • •Previous hip surgery
  • •Pregnancy.

Outcomes

Primary Outcomes

Not specified

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