Postoperative Analgesia Using Ganglion Impar Block After Anal Surgery
ConditionPostoperative Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Alexandria
About this trial
The aim of this study is to evaluate the ganglion Impar block in the prevention of postoperative pain after anal surgery.
Eligibility criteria
Qualifiers
patients undergoing hemorrhoidectomy surgery in Alexandria University hospital.
Disqualifiers
Coagulation effects
Allergy to Bupivacaine
Previous anal surgery
Patient refusal
Trial design
Treatments tested in this trial
- Ganglion impar block with Bupivacaine.
- Ganglion impar block with normal saline
Treatment groups
60 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov