ClinicalTrials.gg
CompletedNCT04067453EASFUpdated Nov 29, 2019

External Anal Sphincter Fatigability

An observational study in External Anal Sphincter Fatigability, sponsored by Gérard Amarenco. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-11-29.

Sponsored by Gérard Amarenco · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
19
Ages
18 Years and older
Sex
All
01

Study summary

External anal sphincter is a Skeletal muscle under voluntary control. As described in previous studies, it is mainly composed of type 1 fibers. Fatigability is a concept which has been studied and described many times in skeletal limbs muscles. Two types of fatigue are described, peripheral of central fatigue. Fatigue can been physiologic but also pathologic (due to an affection of the muscle, the peripheral nervous system or the central nervous system). Many tools have been used to measure muscle fatigability (direct strength measure on isometric contraction, electromyography, echography, oxymetry...).

Besides many fatiguing methods have been developed for every each muscle depending on its histological structure.

Anal sphincter fatigability has already been described in few manometric studies with particularly 2 measures: Fatigue Rate and Fatigue Rate Index. Moreover, no fatiguing protocol has been standardized to study it.

The primary aim of this study is to define a fatiguing protocol for external anal sphincter in order to study it in further studies. Secondary aims are to assess Electromyography as a tool for measuring this fatigability and finally to assess the link between anal sphincter fatigability and symptoms reported by patients.

Patients over 18 years old, consulting for an Anorectal Manometry with a voluntary command on the external anal sphincter are included.

History and treatment, height, weight, sex, age, Fatigue impact scale, digestive symptoms with Neurologic Bowel Disorders score and Wexner scale, urinary tract symptoms with Urinary Symptom Profile (USP) score and electromyography (Root Mean Square (RMS) and Mean Power Frequency (MPF)) and manometric data (contraction peak, fatigue rate, fatigue rate index) were recorded.

The fatiguing protocol consists in 10 sustained external anal sphincter contractions with maximal voluntary contraction of 20 seconds followed by 10 seconds of resting. A training contraction is made before the fatiguing protocol. At the end of the protocol, patients undergo a classical anorectal manometry.

Primary outcome is the difference on root mean square in electromyography between the first and the last fatiguing contraction.

Secondary outcomes were mean power frequency and manometric data (i.e. Fatigue Rate index (FRI), Fatigue Rate (FR), contraction Peak)

Influence of age, sex, symptoms, pathologies, weight on fatigability will be studied in a second analysis

02

Conditions studied

  • External Anal Sphincter Fatigability

Keywords

  • Anal Canal
  • External Anal Sphincter
  • Muscle fatigue
  • Electromyography
  • Anorectal Manometry
03

In context

Lead sponsor

Gérard Amarenco is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

all patients over 18 years old presenting for anorectal manometry examination in order to explore anorectal disorders between 01/08/2019 and 31/10/2019 with a voluntary command on external anal sphincter contraction

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • over 18 years old
  • voluntary command on external anal sphincter contraction during physical examination
  • Anorectal disorders

Exclusion criteria

Exclusion Criteria:

  • inability to understand simple orders
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
19 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients undergoing fatiguing protocol

    patient consulting for anorectal manometry in order to explore anorectal disorders with a voluntary command on external anal sphincter

    Other: Fatiguing contractions

Interventions

  • OtherFatiguing contractions

    10 sustained external anal sphincter contractions with maximal voluntary contraction of 20 seconds followed by 10 seconds of resting.

06

What researchers measure

Primary outcomes

  1. Variation in electromyographic muscle response 1

    Difference between first and last fatiguing contractions on surface electromyographic Root Mean Square (RMS)

    Time frame: 1 day

Secondary outcomes

  1. variation of electromyographic muscle response 2

    Difference between first and last fatiguing contractions on surface electromyographic Mean Power Frequency (MPF)

    Time frame: 1 day

  2. variation of external anal sphincter contractions with manometry 1

    Difference between first and last contractions on manometrical Fatigue rate

    Time frame: 1 day

  3. variation of external anal sphincter contractions with manometry 2

    Difference between first and last contractions on manometrical Fatigue rate Index

    Time frame: 1 day

  4. variation of external anal sphincter contractions with manometry 3

    Difference between first and last contractions on manometrical Peak of Contraction

    Time frame: 1 day

07

Study locations

1 site
  • department of Neuro-Urology, Hôpital Tenon
    Paris, 75020, France
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04067453
Lead sponsor
Gérard Amarenco
Responsible party
Gérard Amarenco (Head of Neuro-Urology department, Tenon Hospital, Pierre and Marie Curie University) — Sponsor-investigator
First posted
Aug 26, 2019
Start date
Aug 1, 2019
Primary completion
Oct 31, 2019
Completion
Nov 2, 2019
Last update
Nov 29, 2019

Study contacts

Gérard Amarenco
principal investigator · Study Principal Investigator Sorbonne Université, GRC 001, GREEN, AP-HP, Hôpital Tenon, Paris, France

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion