Status:

COMPLETED

Intraperitoneal Atomization of Levobupivacaine During Gynaecological Laparoscopic Procedures ; Impact on Pain, Opioid Use and Length of Recovery Room Stay (IPLA).

Lead Sponsor:

University Hospital, Ghent

Conditions:

Pain, Postoperative

Eligibility:

FEMALE

18+ years

Phase:

PHASE4

Brief Summary

In this study, we will compare 3 treatments. The first group of patients will receive the standard treatment (paracetamol, diclofenac and an opioid if necessary) with infiltration of the portal sites ...

Eligibility Criteria

Inclusion

  • Patients who are planned for gynaecological laparoscopic interventions on an ambulatory basis.

Exclusion

  • Less than 18 year old.
  • Weight less than 50 kg and more than 80 kg.
  • Pregnant.
  • Prisoners;
  • Allergic to topical anesthetics (Amides specifically).
  • Allergic to Opioids as a class.
  • Currently or within the last 30 days been prescribed an opiate medication.
  • Chronic pain syndrome.

Key Trial Info

Start Date :

June 26 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 3 2018

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT01886352

Start Date

June 26 2013

End Date

December 3 2018

Last Update

December 5 2018

Active Locations (1)

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Ghent University Hospital

Ghent, Belgium, 9000