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

NCT ID: NCT04043702

Last Updated: 2019-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-01-04

Study Completion Date

2019-07-29

Brief Summary

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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).

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Detailed Description

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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.

Conditions

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Obesity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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on topiramate

"topiramate", "conviban®" group vs no treatment ( control group).

The intervention being studied

Intervention Type DRUG

Intervention Other Names have not been specified

on empagliflozine

"empagliflozine", "jardiance®" vs no treatment ( control group).

The intervention being studied

Intervention Type DRUG

Intervention Other Names have not been specified

on topiramate plus empagliflozine

all patients' vs no treatment ( control group).

The intervention being studied

Intervention Type DRUG

Intervention Other Names have not been specified

no treatment

all patients' vs no treatment ( control group).

The intervention being studied

Intervention Type DRUG

Intervention Other Names have not been specified

Interventions

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The intervention being studied

Intervention Other Names have not been specified

Intervention Type DRUG

Other Intervention Names

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"empagliflozine", "jardiance®") "topiramate", "conviban®"

Eligibility Criteria

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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
Minimum Eligible Age

30 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ministry of Health and Population, Egypt

OTHER_GOV

Sponsor Role lead

Responsible Party

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mahmoud younis

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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mahmoud younis, M.S

Role: PRINCIPAL_INVESTIGATOR

egyptian ministry of health

Locations

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Mahmoud Younis

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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12345678

Identifier Type: -

Identifier Source: org_study_id

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