Comparison Between Single and Triple Rubber Band Ligation for the Treatment of Hemorrhoids

NCT ID: NCT01383577

Last Updated: 2013-09-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-03-31

Study Completion Date

2013-11-30

Brief Summary

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Rubber band ligation is a widely adopted treatment of internal hemorrhoids in busy coloproctology institutions. All three major hemorrhoidal clusters (left lateral, right anterior and right posterior) use to be ligated in order to obtain therapeutic success. It is commonly performed either through the ligation of a single hemorrhoid per session spaced by some few weeks to the second and third sessions, or of all three major hemorrhoids in one single session. Advocates of either method of hemorrhoidal ligation have arguments to defend their choice in terms of advantages, supported mainly on personal preferences. The investigators objective is to determine, through a controlled double-blinded randomized study, if there is any superiority of single hemorrhoidal ligation per session (in a total of three sessions) over the method of ligation of all three main hemorrhoids in a sole session in terms of therapeutic success (resolution of pre-ligation symptoms), morbidity, patient satisfaction and costs (institutional, labor and patient-related).

Detailed Description

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Because of conflicting results in existing literature in relation to features such as pain and immediate effectiveness of single or multiple rubber band ligation of hemorrhoids and because in the literature consulted no study was found that addressed economical features comparing single with multiple rubber band ligation of hemorrhoids, this study was designed to compare, in a double blinded, randomized and controlled model, the results of single hemorrhoidal ligation in three sessions with triple hemorrhoidal in a sole session in terms of immediate effectiveness, patient satisfaction and costs.

Patients enrolled in the study, after applying inclusion and exclusion criteria, signed the consent form, and responded to a questionaire about epidemiological data and hemorrhoidal symptoms, are (and will be) randomly allocated to one of the two arms of the study: G1: a single major hemorrhoidal group is ligated in each of three sessions of hemorrhoidal ligation, while the two other hemorrhoidal groups are submitted to sham ligation (a McGown aspirating type of hemorrhoidal ligator is employed); G2: all three major hemorrhoidal groups are ligated in the first session of treatment and in the next two sessions only sham ligations are performed. Three sessions of hemorrhoidal and/or sham ligation are performed in all patients, each spaced by one month from the other. A final consultation is held 1 month after the third ligation session in order to gather all the results of the treatment.

After each session of hemorrhoidal ligation patients receive a chart containing a modified level of pain scale (Wong \& Baker) and are asked to indicate pain level (from 0 to 5: 0 = no pain, 5 = unbearable pain) at fixed intervals (immediate post-ligation, 12 h post-ligation, 24 h post-ligation and each other day until 7 days post-ligation). Investigators gather this information about pain, and patient well-being post-ligations, from 8 programmed telephone calls to the patients after each session of hemorrhoidal (or sham) ligation.

Three months after the first session of hemorrhoidal ligation all patients are examined in order to observe treatment effectiveness and gather data about complications, patient satisfaction, number of days of occupational absenteeism linked to each session of treatment and number of analgesic pills necessary for pain relief.

Comparative costs of each modality of ligation are raised taking into consideration the salaries of health professionals involved in the treatment, the salaries of the patients (calculation of absenteeism), the value of consumables used in each session of effective ligation, the depreciation price of permanent material employed and the price of medications patients have to buy.

Patients are blinded to the modality of hemorrhoidal ligation employed and the statistician does not know the nature of each treatment group.

Conditions

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Second-degree Hemorrhoids

Keywords

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Hemorrhoids Ligation Pain Morbidity Patient Satisfaction Cost-Benefit Analysis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Single hemorrhoidal ligation

Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each session of treatment.

Group Type EXPERIMENTAL

Single hemorrhoidal ligation

Intervention Type PROCEDURE

Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each of three sessions of treatment. Final revision is performed 90 days after first session of hemorrhoidal ligation.

Triple hemorrhoidal ligation

The three major hemorrhoidal groups are ligated in the first session of ligation. The three following monthly appointments of patients of this arm are for sham hemorrhoidal ligations and final revision.

Group Type EXPERIMENTAL

Triple hemorrhoidal ligation

Intervention Type PROCEDURE

The three major hemorrhoidal groups are ligated in the first session of ligation. Sham triple hemorrhoidal ligations are performed 30 and 60 days after the first session. Final revision is done 90 days after first ligation session.

Interventions

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Single hemorrhoidal ligation

Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each of three sessions of treatment. Final revision is performed 90 days after first session of hemorrhoidal ligation.

Intervention Type PROCEDURE

Triple hemorrhoidal ligation

The three major hemorrhoidal groups are ligated in the first session of ligation. Sham triple hemorrhoidal ligations are performed 30 and 60 days after the first session. Final revision is done 90 days after first ligation session.

Intervention Type PROCEDURE

Other Intervention Names

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Rubber band ligation of hemorrhoids, single Rubber band ligation of hemorrhoids, multiple

Eligibility Criteria

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Inclusion Criteria

* Patients with second-degree hemorrhoids

Exclusion Criteria

* Patients with special needs
* Immunodepression
* Indians
* Infectious, inflammatory or tumoral anorectal comorbidities
* Previous anorectal surgeries
* Patients on anticoagulant therapy or with coagulation disorders
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Federal University of Amazonas

OTHER

Sponsor Role lead

Responsible Party

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Ivan Tramujas da Costa e Silva

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ivan T Costa e Silva, PhD

Role: PRINCIPAL_INVESTIGATOR

Universidade Federal do Amazonas

Érico L Melo, Med Grad

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Giselle L Afonso, Med Grad

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Felicidad S Gimenez, MSc

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Shymmene O Cardoso, BAccount

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Daniel Richard M Mota, Med Grad

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Rachel M Carvalho, Med Grad

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Saskia Regina F Coppens, Med Grad

Role: STUDY_CHAIR

Universidade Federal do Amazonas

Themis C Abensur, MSc

Role: STUDY_CHAIR

Federal University of Amazonas

Locations

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Hospital Universitário Getúlio Vargas - Ambulatório Araújo Lima

Manaus, Amazonas, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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PP-S/0001/2010

Identifier Type: -

Identifier Source: org_study_id