Last reviewed · How we verify

NCT04057079

Comparing Anugel With Gelatine Sponges for Pain Management After Hemoroidectomy

Completed Phase 2 Last updated 15 August 2019
What this trial tests

Phase 2 trial testing Anugel, Hydrogel sponge in Pain, Postoperative in 110 participants. Completed in 1 February 2019.

Timeline
4 April 2014
Primary endpoint
9 July 2018
1 February 2019

Quick facts

Lead sponsorDeep Life Medical Ltd
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment110
Start date4 April 2014
Primary completion9 July 2018
Estimated completion1 February 2019
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Deep Life Medical Ltd

Who can join

Eligibility, any sex, with Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Post-operational pain is the most common problem relating to haemorrhoidectomy. This study aims to evaluate the postoperative effects of Anugel a hydrogel impregnated multi component sponge vs gelatine sponge comparatively.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Pain, Postoperative

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04057079.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing