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The Pro-Chol Study

Study acronym: ProChol
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study First Submitted
This prospective clinical cohort study will include patients with gallstones and abdominal pain scheduled for surgery (laparoscopic cholecystectomy). Data on quality of life, abdominal pain, gallstone disease, and patient characteristics will be collected before surgery. The outcomes will be assessed three months following surgery and will primarily be determinants for resolution of pain. The aim is to make a prediction score that may aid clinicians and patients in decision making about surgery.
Trial Details
NCT Number NCT07245108
Lead Sponsor Nordsjaellands Hospital
Collaborators: Hvidovre University Hospital, Copenhagen University Hospital at Herlev, Aalborg University Hospital, Viborg Regional Hospital, Zealand University Hospital, University Hospital Bispebjerg and Frederiksberg, Regionshospital Nordjylland, Regionshospitalet Viborg, Skive
Conditions
(from sponsor)		 Gallstones, Gallstone Attack, Uncomplicated Cholelithiasis, Cholecystolithiasis
Related terms Cholecystolithiasis, Gallstones
Enrollment 800 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov