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Clinical Trial Summary

Patients with hemorrohoids grade II and III were included. Patients were randomized into 2 groups:

- Experimental group: Patients will receive a treatment with vitamin E ovules, which must be placed inside the annus

- Control group: Patients will receive a treatment with corticoid ointment, with endoanal application

Bleeding, pain and stinging will be evaluated 14 days after beginning the treatment.


Clinical Trial Description

Patients with hemorrohoids grade II and III were included.

Patients were randomized into 2 groups:

- Experimental group: Patients will receive a treatment with vitamin E ovules, which must be placed inside the annus. 1 ovule must be inserted daily during 14 days.

- Control group: Patients will receive a treatment with prednisolone ointment, with endoanal application 3 times per day during 14 days.

Bleeding, pain and stinging will be evaluated 14 days after beginning the treatment. Quantification of pain will be performed following a visual analogic scale ranging from 0 (absence of symptoms) to 100 (unbearable symptoms). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04362384
Study type Interventional
Source Hospital General Universitario Elche
Contact Jaime Ruiz-Tovar
Phone 630534808
Email jruiztovar@gmail.com
Status Not yet recruiting
Phase Phase 3
Start date May 1, 2020
Completion date October 30, 2020

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