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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04274608
Other study ID # TanTockSengH
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date January 1, 2020
Est. completion date July 2022

Study information

Verified date February 2020
Source Tan Tock Seng Hospital
Contact Danson Yeo, MBBS, MRCS, FRCS
Phone +65 81834111
Email danson_xw_yeo@ttsh.com.sg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized controlled trial to compare intra-gastric injection of Botulinum Toxin A (Botox; Allergan Inc. Irvine, Ca, USA) against non-surgical management for obesity (i.e. exercise/diet). Our hypothesis is that intra-gastric injection of Botox into the fundus and body of the stomach will result in greater weight loss than just exercise and diet alone.


Recruitment information / eligibility

Status Recruiting
Enrollment 18
Est. completion date July 2022
Est. primary completion date July 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria:

1. Age 21 to 65yrs old

2. BMI >32.5 (Class II obesity)

Exclusion Criteria:

1. Pregnancy or lactation

2. Known pre-existing neuromuscular disorders or peripheral motor neuropathic disease (e.g. amyotrophic lateral sclerosis, motor neuropathy)

3. Patients with known liver cirrhosis or known esophageal/gastric varices

4. Known eating disorders

5. Known major cardiovascular or pulmonary conditions

6. Previous gastric/bariatric surgery

7. Pathologic changes of the esophagus/stomach/duodenum demonstrated on endoscopy (esophagitis, peptic ulcers, cancer)

8. Known alcohol or drug abuse

9. Known allergy to any ingredients in Botox or allergic reaction to any other botulinum toxin product

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Botulinum toxin type A
Intragastric injection of Botulinum toxin type A
Behavioral:
Weight Management Program
12 week weight management program

Locations

Country Name City State
Singapore Tan Tock Seng Hospital Singapore

Sponsors (1)

Lead Sponsor Collaborator
Tan Tock Seng Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight loss Examine the average weight loss 1 year
Primary Time to weight regain following a single injection of intra-gastric Botox 1 year
Secondary Gut hormone level Ghrelin 1 year
Secondary Gut hormone level ( Leptin) Leptin 1 year
Secondary Satiety index 1 year
Secondary Co-morbidities Diabetes, hypertension, hyperlipidemia 1 year
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