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Glycemic Response to Momordica Charantia in Type 2 Diabetes

Primary Purpose

Type 2 Diabetes

Status
Withdrawn
Phase
Phase 2
Locations
Pakistan
Study Type
Interventional
Intervention
Momordica charantia
starch powder
Sponsored by
Services Hospital, Lahore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring diabetes type 2

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adult Type 2 diabetics with mild degree of hyperglycemia (FBG >126<200 mg/dl)
  2. Absence of serious co-morbid conditions
  3. Patients agreeing to participate in this trial

Exclusion Criteria:

  1. Type 1 diabetics
  2. Pregnancy
  3. Paediatric age group
  4. Patients known to be allergic to Momordica charantia
  5. Serious cardio-respiratory illness, previous myocardial infarction, angina pectoris, heart failure, uncontrolled hypertension ≥ stage 2, COPD, asthma, active pulmonary tuberculosis
  6. Significant hepatic impairment: ALT >60, Bilirubin >2 mg/dl
  7. Significant renal impairment: S/creatinine >1.5 mg/dl, albuminuria > 1+
  8. Patients with conditions likely to interfere with the absorption of the trial therapy: malabsorption, chronic diarrhoea, intestinal resection, blind loop syndrome
  9. Patients withholding consent
  10. Patients, both male and female, desiring pregnancy during the trial phase.
  11. Secondary causes of diabetes
  12. Patients using drugs influencing glucose metabolism: steroids, hormonal contraception, menopausal HRT , diazoxide, phenytoin, colchicine

Sites / Locations

  • Services Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Momordica charantia

Arm Description

placebo powder (wheat flour) The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.

Thirty patients will be assigned to each arm in a double blind manner. The active arm will be administered capsules containing a total of 500 mg of Momordica charantia freeze dried powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3. The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.

Outcomes

Primary Outcome Measures

serum fructosamine at end of trial phase in each of the groups

Secondary Outcome Measures

Development of major adverse effects (e.g. intractable vomiting, jaundice, allergic reactions or other effects requiring cessation of therapy and breaking of study code)
GLP-1[7-36] in each group at the end of trial phase
FBG at end of trial phase in each of the groups
HOMA-IR in each of the two groups at end of trial phase
Insulin resistance by the hyperinsulinemic, euglycemic clamp in a subset at the end of trial phase

Full Information

First Posted
January 15, 2009
Last Updated
June 9, 2012
Sponsor
Services Hospital, Lahore
Collaborators
University of the Punjab
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1. Study Identification

Unique Protocol Identification Number
NCT00823953
Brief Title
Glycemic Response to Momordica Charantia in Type 2 Diabetes
Official Title
The Effect of Momordica Charantia on Glycemic Control and Insulin Resistance in Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Withdrawn
Why Stopped
IP could not be made available in sufficient quantity for the expected enrollment
Study Start Date
November 2008 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
February 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Services Hospital, Lahore
Collaborators
University of the Punjab

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetes is a common disease which has been treated by traditional medicines for centuries before modern medicine became available. A very common remedy for Diabetes Mellitus in different cultures is momordica charantia (karela or Bitter gourd). The use of alternative medicine is common among Pakistani population. This study was planned to find out the effect of administering freeze dried powder of momordica charantia for three weeks on the glycemic profile and insulin resistance of treatment naiive patients with mild Type 2 diabetes.
Detailed Description
Momordica charantia is a commonly consumed vegetable, which has formed a part of subcontinental diet since centuries. It has been traditionally used to treat diabetes across three continents, and its glycemic effect has been investigated in a few unblinded trials, but so far no properly designed double blind investigation of its action on insulin resistance has not been carried out. In this study, a randomised placebo controlled double-blind trial will be carried out on mild type 2 diabetic patients, to study the effect of escalating doses of Momordica charantia administered in the form of capsules for the trial phase of three weeks, on glycemic control and parameters of insulin resistance in type 2 diabetes. Among the parameters to be tested will be glucose indices and lipid profile and insulin levels. The effect of Momordica charantia administration on insulin resistance will be assessed using HOMA-IR model and/ or the hyperinsulinemic, euglycemic clamp. The selection of patients with mild hyperglycemia will be done to offset the glucose spill-off effect which occurs beyond the real threshold, and makes the glucose tolerance curve non-linear beyond this level.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
diabetes type 2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo powder (wheat flour) The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.
Arm Title
Momordica charantia
Arm Type
Active Comparator
Arm Description
Thirty patients will be assigned to each arm in a double blind manner. The active arm will be administered capsules containing a total of 500 mg of Momordica charantia freeze dried powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3. The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.
Intervention Type
Drug
Intervention Name(s)
Momordica charantia
Other Intervention Name(s)
Bitter Melon Capsule
Intervention Description
escalating doses of Momordica charantia administered in the form of capsules for the trial phase of three week.Dose level 1: capsules containing a total of 500 mg of freeze dried powder of Momordica charantia. Dose level 1: capsules containing a total of 1000 mg of freeze dried powder of Momordica charantia. Dose level 3: capsules containing a total of 1500mg of freeze dried powder of Momordica charantia.
Intervention Type
Other
Intervention Name(s)
starch powder
Intervention Description
The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.
Primary Outcome Measure Information:
Title
serum fructosamine at end of trial phase in each of the groups
Time Frame
three weeks
Secondary Outcome Measure Information:
Title
Development of major adverse effects (e.g. intractable vomiting, jaundice, allergic reactions or other effects requiring cessation of therapy and breaking of study code)
Time Frame
three weeks
Title
GLP-1[7-36] in each group at the end of trial phase
Time Frame
three weeks
Title
FBG at end of trial phase in each of the groups
Time Frame
three weeks
Title
HOMA-IR in each of the two groups at end of trial phase
Time Frame
three weeks
Title
Insulin resistance by the hyperinsulinemic, euglycemic clamp in a subset at the end of trial phase
Time Frame
3 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult Type 2 diabetics with mild degree of hyperglycemia (FBG >126<200 mg/dl) Absence of serious co-morbid conditions Patients agreeing to participate in this trial Exclusion Criteria: Type 1 diabetics Pregnancy Paediatric age group Patients known to be allergic to Momordica charantia Serious cardio-respiratory illness, previous myocardial infarction, angina pectoris, heart failure, uncontrolled hypertension ≥ stage 2, COPD, asthma, active pulmonary tuberculosis Significant hepatic impairment: ALT >60, Bilirubin >2 mg/dl Significant renal impairment: S/creatinine >1.5 mg/dl, albuminuria > 1+ Patients with conditions likely to interfere with the absorption of the trial therapy: malabsorption, chronic diarrhoea, intestinal resection, blind loop syndrome Patients withholding consent Patients, both male and female, desiring pregnancy during the trial phase. Secondary causes of diabetes Patients using drugs influencing glucose metabolism: steroids, hormonal contraception, menopausal HRT , diazoxide, phenytoin, colchicine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Khadija I Khawaja, MBBS,FCPS
Organizational Affiliation
Services Hospital, Lahore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Services Hospital
City
Lahore
State/Province
Punjab
ZIP/Postal Code
54000
Country
Pakistan

12. IPD Sharing Statement

Citations:
PubMed Identifier
9716917
Citation
Ahmed I, Adeghate E, Sharma AK, Pallot DJ, Singh J. Effects of Momordica charantia fruit juice on islet morphology in the pancreas of the streptozotocin-diabetic rat. Diabetes Res Clin Pract. 1998 Jun;40(3):145-51. doi: 10.1016/s0168-8227(98)00022-9.
Results Reference
background
PubMed Identifier
11269887
Citation
Ahmed I, Lakhani MS, Gillett M, John A, Raza H. Hypotriglyceridemic and hypocholesterolemic effects of anti-diabetic Momordica charantia (karela) fruit extract in streptozotocin-induced diabetic rats. Diabetes Res Clin Pract. 2001 Mar;51(3):155-61. doi: 10.1016/s0168-8227(00)00224-2.
Results Reference
background
PubMed Identifier
17493509
Citation
Dans AM, Villarruz MV, Jimeno CA, Javelosa MA, Chua J, Bautista R, Velez GG. The effect of Momordica charantia capsule preparation on glycemic control in type 2 diabetes mellitus needs further studies. J Clin Epidemiol. 2007 Jun;60(6):554-9. doi: 10.1016/j.jclinepi.2006.07.009. Epub 2006 Nov 13.
Results Reference
background
Links:
URL
http://www.rain-tree.com/bitmelon.htm
Description
Database File for Momordica charantia

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Glycemic Response to Momordica Charantia in Type 2 Diabetes

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