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Electrophysiological and manometric investigations of the Oddi sphincter

Electrophysiological and manometric investigations of the Oddi sphincter

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106510
Enrollment
Unknown
Registered
2025-07-24
Start date
2008-07-03
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sphincter of Oddi dysfunction

Interventions

Control group:Narditest test and Anisodamine
Sphincter of Oddi Dysfunction group:Narditest test and Anisodamine

Sponsors

Southwest Hospital, Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Selection criteria for healthy volunteers 1. Age 20-60 years old, regardless of gender 2. Routine examination of liver function, liver enzyme profile and B-ultrasound without abnormal findings. 3. Voluntarily take the test and sign the informed consent form. 4. Fasting and water abstinence for 12 hours before the test. Inclusion criteria for patients with clinically suspected SOD 1. Patients have a history of cholecystectomy and must have episodic epigastric and/or right upper quadrant pain with all of the following: (1) Abdominal pain lasts for at least 30 minutes (2) Symptoms are intermittent and recurrent, with varying intervals (non-daily attacks) (3) Pain worsens to a relatively stable level (4) The pain is moderate or severe, affecting the patient's daily life or causing the patient to seek medical attention in the emergency department (5) Abdominal pain does not relieve after defecation (6) Abdominal pain is not relieved by changes in body position (7) Antacids do not relieve abdominal pain 2. It may be accompanied by transient jaundice and recurrent pancreatitis 3. Exclude organic lesions of the hepatobiliary system 4. Exclude other systemic organic diseases that can cause abdominal pain

Exclusion criteria

Exclusion criteria: 1.Patients with impaired cardiac or pulmonary function who cannot tolerate the procedure. 2.Patients who have taken any antispasmodic medications within 3 days prior to the examination. 3.Patients with poor compliance or inability to complete the required study protocol.

Design outcomes

Primary

MeasureTime frame
Oddi sphincter electromyography amplitude;Oddi sphincter electromyographic duration;Oddi sphincter electromyographic frequency;Oddi sphincter basal pressure;Oddi sphincter contraction peak;Oddi sphincter contraction duration;

Countries

China

Contacts

Public ContactChen Fei, Li Hucheng, Dong Jiahong

Southwest Hospital, Third Military Medical University

lhca03325@btch.edu.cn+86 138 0118 3213

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026