Clinical Trials Directory

Trials / Completed

CompletedNCT01329796

Pertubation With Lignocaine in Endometriosis

Pertubation With Lignocaine in Endometriosis Associated Symptoms Effect Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Isifer AB · Industry
Sex
Female
Age
21 Years
Healthy volunteers
Not accepted

Summary

Endometriosis is a disease of unknown aetiology that can cause severe dysmenorrhea. An altered immune system with elevated levels of cytokines in the peritoneal fluid as well as increased density of nerve fibres, might explain the pathophysiology of dysmenorrhea in endometriosis patients. Lignocaine has anti-inflammatory properties and exerts effect on nerve endings and intra peritoneal macrophages. Pertubation with lignocaine might represent an alternative treatment for endometriosis related dysmenorrhea and avoids the side-effects related to hormonal treatments. A double blind randomized clinical trial, was carried out to evaluate pertubation with lignocaine as a therapy for dysmenorrhea.

Conditions

Interventions

TypeNameDescription
DRUGLignocaineIntrauterine flushing, pertubation, three treatments given preovulatory at cycle day 6-12 in three sequential menstrual cycles.
DRUGRingers SolutionIntrauterine flushing, pertubation, given preovulatory at cycle day 6-12 in three sequential menstrual cycles.

Timeline

Start date
2007-03-01
Primary completion
2009-06-01
Completion
2010-03-01
First posted
2011-04-06
Last updated
2011-04-06

Locations

3 sites across 1 country: Sweden

Source: ClinicalTrials.gov record NCT01329796. Inclusion in this directory is not an endorsement.