Comparing Anugel With Gelatine Sponges for Pain Management After Hemoroidectomy
Pain, Postoperative
About this trial
This is an interventional supportive care trial for Pain, Postoperative focused on measuring Hemoroidectomy
Eligibility Criteria
Inclusion Criteria:
- Haemorrhoid (grade 3-4)
Exclusion Criteria:
- Repeating cases, additional (non haemorrhoid related) complications
Sites / Locations
- Memorial Sisli Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Anugel
Sponge
In this arm, after the surgery a hydrogel impregnated sponge will be placed in the rectum. The patient is evaluated after the operation and the following day when the sponge is removed. A hydrogel impregnated foam pad is applied on the surface of the wound the following 5 days. The patient is evaluated on post op, on day 1 (usually before discharge) and day 5 The pain of the patients are evaluated according to the VAS scale and the use of analgesics and opioids is monitored.
Currently used treatment method i.e. insertion of gelatine sponge in to the rectum post operation. The patient is evaluated on post op, on day 1 (usually before discharge) and day 5 The pain of the patients are evaluated according to the VAS scale and the use of analgesics and opioids is monitored.