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Endosonograpic Monitoring of Injury to the Anal Sphincter After Transanal Stapled Anastomosis

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Medical University of Vienna

Status

Enrolling

Conditions

Transanal Stapled Anastomosis

Treatments

Device: Transanal stapling device

Study type

Observational

Funder types

Other

Identifiers

NCT05992948
2192/2019

Details and patient eligibility

About

Investigation of the sphincter muscles after low anterior or anterior rectum resection, and sigma resection operation by endoluminal ultrasound and manometrical examination.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Age 18 - 90 years, undergoing transanal stapled anastomosis at the Department of General Surgery, Medical University of Vienna

  • Ability and willingness to understand and comply with study interventions and restrictions.
  • Voluntarily signed informed consent after full explanation of the study to the participant.

Exclusion criteria

  • Any physical or mental disorder, which could interfere with the participant's safety during the clinical trial or with the study objectives
  • Inability to communicate well with the investigator due to language problems or reduced mental development
  • Inability or unwillingness to give written informed consent

Trial contacts and locations

1

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Central trial contact

Christopher Dawoud, MD

Data sourced from clinicaltrials.gov

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