Efficacy of Curcuma longa in treatment of postprandial distress syndrome: an open-label randomized controlled trial

Phase 3

Completed

• Conditions: Postprandial distress syndrome; Postprandial distress syndrome, dyspepsia, satiety, epigastric fullness, bloating

• Registration Number: TCTR20180131001
• Lead Sponsor: icharat Sawangroj

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-01-31
• Study Completion: 2019-01-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 78

Inclusion Criteria

- Patients with PDS of functional dyspepsia according to ROME IV criteria including uninvestigated dyspepsia
- No alarm features
- Discontinued all GI medications for 1 week

Exclusion Criteria

- Drugs allergy (simethicone and/or Curcuma longa)
- Pregnancy/lactation
- History of gastric malignancy
- History of gallstone or biliary obstruction

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Global overall symptom scale of dyspepsia 4 weeks 7-point Likert scale

Secondary Outcome Measures

Name	Time	Method
Rate of recurrence 6 weeks record in diary ,time of recurrence 6 weeks record in diary ,side effects 4 weeks record in diary