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The safety and efficacy of one-off electronic colonoscopy in lower gastrointestinal tract examination: an observational clinical research.

The safety and efficacy of one-off electronic colonoscopy in lower gastrointestinal tract examination: an observational clinical research.

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045070
Enrollment
Unknown
Registered
2021-04-05
Start date
2021-04-05
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

Disease of lower digestive tract

Interventions

Observation Group:no

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-75 years, gender unlimited; 2.Electronic colonoscopy required; 3.Voluntary participation in this clinical trial, has signed a written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with contraindications to colonoscopy: (1)Patients with abdominal cavity aneurysm; (2)Those with peritonitis or symptoms of intestinal perforation; (3)Severe cardiovascular and cerebrovascular diseases; (4)Patients with acute radiation colitis; (5)Late-stage tumors with pelvic metastasis and/or obvious ascites; (6)Severe and extensive adhesions after abdominal or pelvic surgery; (7)Patients with combined systemic bleeding diseases, or abnormal blood coagulation function with bleeding tendency; (8)Female patients during menstruation; (9)Those who suffer from mental illness or severe intellectual disability who cannot cooperate with endoscopy; (10)Those with huge diverticulum in the colon; 2.Those who have a history of colectomy; 3.Pregnant and lactating women; 4.Emergency colonoscopy and/or treatment; 5.Participants in other clinical trials 1 month before screening; 6.Those who have a history of allergies to anesthetics; 7.The researcher believes that it is not suitable to participate in this trial.

Design outcomes

Secondary

MeasureTime frame
Evaluation of clinical experience;Instrument failure/defect rate;

Primary

MeasureTime frame
Image Quality;

Countries

China

Contacts

Public ContactHuang Jie'an

The Second Affiliated Hospital of Guangxi Medical University

hjagxmu@163.com+86 13471181378

Outcome results

None listed

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