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Effect of Aloe vera capsule in control of gastroesophageal reflux disease

To evaluate the efficacy and safty of Aloe vera capsule in gastroesophageal reflux disease patients and comparing the control of symptoms with pantoprazole

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080901001165N42
Enrollment
120
Registered
2019-11-30
Start date
2019-12-21
Completion date
Unknown
Last updated
2019-12-17

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

Conditions

gastroesophageal reflux disease. Diseases of oesophagus, stomach and duodenum

Interventions

Intervention 1: Intervention group: Aloe Vera capsule for 28 day, twice a day and pantoprazole for 28 day, once a day. Intervention 2: Control group: pantoprazole for 28 day, once a day. Intervention

Sponsors

Tabib daru pharmaceutical company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Obtaining the informed consent of the patient. Diagnosis of reflux has been confirmed by a physician Considering clinical and para clinical findings. The patient's condition is not life-threatening.

Exclusion criteria

Exclusion criteria: Have been treated with any interactive medication before intervention; such as H2 blocker inhibitors and herbal medicines or drugs that are harmful to treatment for reflux such as theophylline and the like. Participate in another clinical trial at the same time. Pregnancy

Design outcomes

Primary

MeasureTime frame
Bloat. Timepoint: Before intervention, 2 and 4 weeks after intervention. Method of measurement: Questionnaire.;Nausea and vomiting. Timepoint: Before intervention, 2 and 4 weeks after intervention. Method of measurement: Questionnaire.;Heartburn. Timepoint: Before intervention, 2 and 4 weeks after intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: Before intervention, 2 and 4 weeks after intervention. Method of measurement: Heartburn/Reflux Symptoms Questionnaire.;Drug Adverse effects. Timepoint: After prescription of drug. Method of measurement: Data form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYunes Panahi

Bagheiat-allah University of Medical Sciences

Yunespanahi@bmsu.ac.ir+98 21 8248 2503

Outcome results

None listed

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