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Risk factors of dyspepsia after cholecystectomy and establishment and evaluation of the clinical prediction model

Risk factors of dyspepsia after cholecystectomy and establishment and evaluation of the clinical prediction model

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102484
Enrollment
Unknown
Registered
2025-05-15
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Biliary diseases

Interventions

Control group:None
Disease group:None

Sponsors

Ordos Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18–70 years; (2) Post-LC (Laparoscopic Cholecystectomy) patients, including those who underwent cholecystectomy due to cholecystitis, gallstones, gallbladder polyps, other benign gallbladder tumors, or non-functioning gallbladder;** (3) Prospective patients must sign informed consent forms and agree to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Patients with severe cardiac, pulmonary, or renal dysfunction; (2) Neurological or psychiatric disorders, or inability to cooperate with the study for other reasons; (3) Advanced malignant tumors or other severe wasting diseases, any unstable chronic or acute conditions; (4) Previous history of gastrointestinal disorders; (5) Patients with imaging-confirmed dyspepsia caused by biliary obstruction, biliary fluid accumulation, or other biliary tract-related causes (e.g., ultrasound findings); (6) Acute hepatitis or other active liver diseases; (7) Patients lost to follow-up due to various reasons.

Design outcomes

Primary

MeasureTime frame
Gallbladder size;

Secondary

MeasureTime frame
The number of gallbladder stones;Body mass index(BMI);Thickness of the gallbladder wall;

Countries

China

Contacts

Public ContactCao Xi

Ordos Central Hospital

21969644@qq.com+86 150 4988 0146

Outcome results

None listed

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