Normative Metrics of High-Resolution Anorectal Manometry With the Use of Water-perfused System in a Healthy Russian Cohort

Healthy Subjects Clinical Trial

Official title:

Study of Normative Metrics of High-resolution Anorectal Manometry With the Use of Water-perfused Catheter in a Russian Population Without Signs of Functional and Organic Anorectal Disorders

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03897296
• Other study ID #: HRAM-HV
• Status: Recruiting
• Phase: N/A
• Start date: April 15, 2019
• Est. completion date: April 15, 2024

Study information

• Verified date: February 2022
• Source: Russian Academy of Medical Sciences
• Contact: Sergey Morozov, MD, PhD
• Phone: +74996131091
• Email: morosoffsv[@]mail.ru
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

High resolution anorectal manometry (HRAM) normative values are still need to be studied in different populations and with the use of different (solid-state and water-perfused) systems. No studies on HRAM normative values in a Russian population without signs of functional and organic anorectal pathology has been carried out yet.

Description:

High-resolution anorectal manometry (HRAM) is a modern technique used to evaluate the function of the rectum and its sphincters. It is intended to measure the resting pressure in the anal canal, as well as pressure during voluntary contraction of the external anorectal sphincter and pelvic floor muscles and to evaluate reactions to the functional tests.

Several studies have been performed to evaluate normative metrics of anorectal manometry to the moment, but most of them enrolled patients living in the US and countries of the Western Europe. Nutritional patterns, ethnic composition of the population and other factors may cause the differences in the mormative values of HRAM in different populations. Current study is organized to evaluate normative metrics of HRAM in a Russian healthy cohort.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: April 15, 2024
• Est. primary completion date: April 15, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Willingness to participate in this clinical trial, confirmed by signed informed consent form.

• Patients of both sexes, aged 18 to 65 years inclusive.

• Permanent residence in the Russian Federation (capable citizens of Russia on the basis of a passport of a citizen of the Russian Federation).

• Absence of rectal diseases, confirmed by the results of clinical and instrumental examinations

• Ability to follow the instructions when high-resolution anorectal manometry procedure is performed.

Exclusion Criteria:

• Known diseases of the rectum on the basis of clinical and / or instrumental examination, including presence of complaints to difficulties with defecations that require manual aids or use of laxatives;

• Surgical interventions on pelvic organs in history;

• History of organ transplantation except for corneal transplantation and eye lens replacement surgery;

• Oncology of any localization, with the exception of skin cancer in situ;

• Severe concomitant pathology of any organs and systems, which, in the opinion of the researcher, makes it impossible to carry out the procedure of high-resolution anorectal manometry or if the procedure may cause the risk of worsen the patient's condition;

• Absence of anamnestic, clinical and laboratory signs of alcohol abuse (abuse will be considered in case of the use of more than 30 g of pure alcohol per day by males and the use of more than 20 g of pure alcohol per day by females;

• Use of illegal drugs, including history;

• Use of concomitant medications that can affect the motor function of the colon (including, but not limited to: calcium channel blockers, metoclopramide, m-cholinolytics, domperidone, nitrates, tricyclic antidepressants, opiates, beta-blockers, beta-adrenomimetics, alcohol). The duration of the period of non-use of these drugs should provide sufficient time for the complete cessation of their pharmacological action, but not less than two half-life periods.

• Pregnancy and breast-feeding;

• Technical impossibility to insert the catheter due to the previously known or current poor tolerability of high-resolution anorectal manometry procedure or due to the presence of anatomical features that make it impossible to insert the catheter.

Criteria of non-inclusion of the data to the analysis:

• Patients may choose to stop their participation in the study by withdrawal of their previously signed consent, that leads to the exclusion of their data from the analysis.

The researcher should be guided by the following criteria, however, he may at any time terminate the patient's participation in the study on the basis of his own clinical judgment.

Cancellation of participation in the study can be carried out on the basis of the following events:

1. Lack of the possibility to insert water-perfused catheter during high-resolution anorectal manometry procedure due to anatomical features or psychological state of the patient.

2. Incomplete high-resolution anorectal manometry procedure.

3. Presence of adverse event(s) during high-resolution anorectal manometry procedure, causing the further procedure impossible.

4. Obtaining incomplete recording of high-resolution anorectal manometry parameters for any reason.

5. Identification of the conditions described in the section "exclusion criteria" during examination of the patient.

Related Conditions & MeSH terms

• Healthy Subjects

Intervention

Diagnostic Test:
• High resolution anorectal manometry, water perfused catheter
High resolution anorectal manometry with the use of water-perfused catheter will be performed to eligible subjects willing to participate in the study

Locations

Country	Name	City	State
Russian Federation	Gastroenterology and Hepatology, FRC Nutrition and Biotechnology	Moscow
Russian Federation	State Scientific Center of Coloproctology	Moscow

Sponsors (3)

Lead Sponsor	Collaborator
Russian Academy of Medical Sciences	Federal Research Centre of Nutrition and Biotechnology, State Scientific Centre of Coloproctology, Russian Federation

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Resting anorectal pressure obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Anorectal pressure at rest, mm Hg	1 minute
Primary	Maximal squeeze pressure obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Maximal pressure when a squeeze test is performed, mm Hg	5 seconds
Primary	Maximal pressure of endurance squeeze test performed with the use of water-perfused catheter for high-resolution anorectal manometry	mean pressure during test, mm Hg	30 seconds
Primary	Push test pressure obtained with the use of water-perfused catheter for high-resolution anorectal manometry	mean pressure during push test, mm Hg	5 seconds
Primary	Cough test	Cough test pressure, maximal	5 seconds
Primary	Pressure of the first sensation obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Pressure of the first sensation by the test of reservoir function of the rectum, mm Hg	1 minute
Primary	Pressure of the urge to defecate obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Pressure of the urge to defecate by the test of reservoir function of the rectum, mm Hg	1 minute
Primary	Maximal tolerate volume pressure obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Maximal tolerate volume pressure by the test of reservoir function of the rectum, ml	1 minute
Primary	First pain sensation pressure obtained with the use of water-perfused catheter for high-resolution anorectal manometry	Appearance of pain sensation by the test of reservoir function of the rectum, mm Hg	1 minute