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Effect of traditional medicine product based on Rosa damascena on gastroesophageal reflux disease (GERD)

Effect of traditional medicine product based on Rosa damascena on gastroesophageal reflux disease (GERD): a double-blind clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200303046677N5
Enrollment
70
Registered
2021-01-16
Start date
2021-02-19
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

gastroesophageal reflux. Gastro-esophageal reflux disease

Interventions

Intervention 1: Control group: Placebo, this capsule is prepared in Tuba Green Gold Pharmaceutical Company and medicinal corn starch is used as a placebo, which is filled in capsules of the same color

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: With reflux at the age of 18 to 80 years

Exclusion criteria

Exclusion criteria: Having a history of Barrett's esophagus History of esophageal or gastric surgery History of esophageal, gastric or abdominal cancer Having coagulation problems that prevent them from stopping their medication Patients receiving regular glucocorticoids and nonsteroidal anti-inflammatory drugs more than three days a week for the past 28 days Receiving sucralfate three days before enrollment Take aspirin daily at a dose of more than 150 mg Acute peptic ulcer or its complications Receive antibiotic treatment to eradicate Helicobacter Pylori in the last 28 days Smoking or Alcohol

Design outcomes

Primary

MeasureTime frame
Heartburn. Timepoint: On arrival, the second week and fourth week. Method of measurement: Questionnaire.;Reflux throat. Timepoint: On arrival, the second week and fourth week. Method of measurement: Questionnaire.;Pain in the middle and upper stomach. Timepoint: On arrival, the second week and fourth week. Method of measurement: Questionnaire.;Nausea. Timepoint: On arrival, the second week and fourth week. Method of measurement: Questionnaire.;Difficulty in falling asleep due to reflux symptoms. Timepoint: On arrival, the second week and fourth week. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasool Choopani

Shahid Beheshti University of Medical Sciences

rchoopani@sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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