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NCT04043702 Clinical Trial

Combination of Topiramate and Empagliflozin is Considered a Good Option for the Treatment of Obesity

Obesity Clinical Trial

Official title:
Combination of Topiramate(Conviban) and Empagliflozin(Jardiance) is Considered a Good Option for the Treatment of Obesity

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04043702
Other study ID # 12345678
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 4, 2019
Est. completion date July 29, 2019

Study information
Verified date August 2019
Source Ministry of Health and Population, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim was to show if a combination of topiramate and empagliflozin have the greatest weight decreasing effect in comparison to each drug alone and to group with no treatment( control group).

.

Description:

The aim was to show if a combination of topiramate and empagliflozin have the greatest weight decreasing effect in comparison to each drug alone and to group with no treatment( control group).

Materials and methods 200 obese patients 4 groups. had been monitored in a private clinic, each group 50 patients number, with 35 females and 15 males who were already on treatment.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date July 29, 2019
Est. primary completion date July 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 55 Years
Eligibility Inclusion Criteria:

1. stable weight in the previous 6 months.

2. a sedentary lifestyle.

3. no history of diabetes mellitus.

4. taking medication that affects appetite, or weight within the past 6 months

Exclusion Criteria:

1. severe anemia

2. hypothyroidism and hyperthyroidism

3. Diabetes mellitus

4. moderate to severe liver or kidney disease

5. body mass index less than 30

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• The intervention being studied
Intervention Other Names have not been specified

Locations
Country Name City State
Egypt Mahmoud Younis Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ministry of Health and Population, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in weight weight measurement 6 months
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