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Clinical Study to Evaluate Antihyperlipidemic Effect of a Classical Unani Antiobesity Formulation

Primary Purpose

Hyperlipidemia

Status
Completed
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
safoof e muhazzil
compressed tablet of safoof e muhazzil
Atorvastatin
Sponsored by
Jamia Hamdard University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperlipidemia focused on measuring TC, TG, HDL, LDL, VLDL

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 20 Year(s) To 70 Year(s)
  • Gender Both
  • participate in Clinical Trial voluntarily.
  • Hyperlipidemic

Exclusion Criteria:

  • Persons below 20 yrs and Above 70 yrs of age
  • Pregnancy
  • Liver diseases
  • Renal diseases
  • Diabetes mellitus Type II
  • Alcoholic
  • AIDS
  • Thyroid Disease
  • Drug intake ? Corticosteroids, Diuretics, Beta-blockers, Oral contraceptives, Cyclosporin, Androgens & Retinoids

Sites / Locations

  • Majeedia Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Safoof e Muhazzil in its conventional powder form

compressed tablet of safoof e muhazzil

atorvastatin

Arm Description

safoof e muhazzil in its conventional powder form 5 gms twice daily given orally

compressed tablet of safoof e muhazzil is given in equivalent dose orally

atorvastatin 10mg daily as a standard control

Outcomes

Primary Outcome Measures

Total Cholesterol (TC)
Low density Lipoprotein (LDL)
Triglycerides (TG)
High Density Lipoprotein (HDL)
Very Low Density Lipoprotein (VLDL)

Secondary Outcome Measures

Waist to Hip ratio
Body Mass Index

Full Information

First Posted
April 5, 2011
Last Updated
October 18, 2014
Sponsor
Jamia Hamdard University
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1. Study Identification

Unique Protocol Identification Number
NCT01332747
Brief Title
Clinical Study to Evaluate Antihyperlipidemic Effect of a Classical Unani Antiobesity Formulation
Official Title
Clinical Study on Hyperlipidemia and Comparative Evaluation of Efficacy of a Compound Unani Formulation (Safoof e Muhazzil) and Compressed Tablet of Safoof e Muhazzil in Its Management
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jamia Hamdard University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this clinical trial is to study the comparative effect of a classical unani antiobesity drug safoof-e-muhazzil on hyperlipidemia in its classical powder form and in compressed tablet form against a standard control.
Detailed Description
The largest proportion of cardiovascular diseases is represented by Coronary artery disease(CAD), cerebral and peripheral vascular diseases. During the past decades efficacious strategies have been developed for prevention of these diseases. These strategies involve general lifestyle changes, which include, healthy diet, optimal weight, physical activity, moderate or no alcohol consumption, and smoking cessation, treatment of high blood pressure, control of diabetes mellitus and in particular, treatment of hyperlipidemia. Major clinical trials carried out, have shown a clear benefit of low density lipoprotein-cholesterol(LDL-C) reduction in terms of both CAD events and total mortality. A similar reduction in the relative risk of coronary events has been documented in patients with and without clinically evident CAD and in patients with mild or severe hyperlipidemia. Hyperlipidemia can be primary which is gene related causing defects in the synthesis of lipoprotein degradation. The other type of hyperlipidemia is secondary which is subsequent to related metabolic abnormalities. Although several Unani physicians have mentioned considerable details about fats in blood but it is observed that Hyperlipidemia has not been mentioned per se in the classical Unani literature. A condition that resembles hyperlipidemia in various aspects like etiology, clinical features and complications has been described as obesity in the classical Unani literature and mentions related methods for managing such disorders including regimens and drugs (for reducing weight) are also observed in such references. Unani physicians have bracketed obesity under cold derangement of temperament. Unani physicians have emphasized the effect of Safoof-e-Muhazzil as the main weight loss drug. Furthermore, Many of the drugs present in Safoof-e-Muhazzil including Lac which itself is a constituent of Safoof-e-Muhazzil have been attributed by Unani physicians to have de obstruent, desiccant, and softening and relaxant effect on vessel walls properties which further supports our hypothesis. These properties are also in cohesion with our hypothesis and perhaps these drugs may have scraping effect on atherosclerotic vessel walls. Lipids are metabolized mainly in the liver and it is the error of the liver or the weakness of the liver that these lipids go unchecked into the blood stream. Since most of constituents of Safoof-e-Muhazzil including Lac have been attributed to be liver strengthening agents, hence, due to their corrective effect on liver may help correcting raised lipid levels in the blood.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperlipidemia
Keywords
TC, TG, HDL, LDL, VLDL

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
128 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Safoof e Muhazzil in its conventional powder form
Arm Type
Experimental
Arm Description
safoof e muhazzil in its conventional powder form 5 gms twice daily given orally
Arm Title
compressed tablet of safoof e muhazzil
Arm Type
Experimental
Arm Description
compressed tablet of safoof e muhazzil is given in equivalent dose orally
Arm Title
atorvastatin
Arm Type
Active Comparator
Arm Description
atorvastatin 10mg daily as a standard control
Intervention Type
Drug
Intervention Name(s)
safoof e muhazzil
Intervention Description
drug is composed of 5 herbal(Carum Carvi,Trachyspermum copticum,Foeniculum Vulgare,Origanum Vulgare,Ruta Graveolens) 1 animal origin (Lac)and 1 mineral origin (Borax) ingredients. to be given in a dosage of 5 gms twice daily
Intervention Type
Drug
Intervention Name(s)
compressed tablet of safoof e muhazzil
Intervention Description
drug is composed of 5 herbal(Carum Carvi,Trachyspermum copticum,Foeniculum Vulgare,Origanum Vulgare,Ruta Graveolens) 1 animal origin (Lac)and 1 mineral origin (Borax) ingredients. compressed into tablets of 1 gm each+ binders qs. dose is 5 tablets twice daily
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Intervention Description
atorvastatin 10 mgs once daily
Primary Outcome Measure Information:
Title
Total Cholesterol (TC)
Time Frame
six weeks
Title
Low density Lipoprotein (LDL)
Time Frame
six weeks
Title
Triglycerides (TG)
Time Frame
six weeks
Title
High Density Lipoprotein (HDL)
Time Frame
six weeks
Title
Very Low Density Lipoprotein (VLDL)
Time Frame
six weeks
Secondary Outcome Measure Information:
Title
Waist to Hip ratio
Time Frame
six weeks
Title
Body Mass Index
Time Frame
six weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 20 Year(s) To 70 Year(s) Gender Both participate in Clinical Trial voluntarily. Hyperlipidemic Exclusion Criteria: Persons below 20 yrs and Above 70 yrs of age Pregnancy Liver diseases Renal diseases Diabetes mellitus Type II Alcoholic AIDS Thyroid Disease Drug intake ? Corticosteroids, Diuretics, Beta-blockers, Oral contraceptives, Cyclosporin, Androgens & Retinoids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Umar Jahangir, MD Scholar
Organizational Affiliation
Jamia Hamdard
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Asim Ali Khan, MD
Organizational Affiliation
Jamia Hamdard
Official's Role
Principal Investigator
Facility Information:
Facility Name
Majeedia Hospital
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110062
Country
India

12. IPD Sharing Statement

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Clinical Study to Evaluate Antihyperlipidemic Effect of a Classical Unani Antiobesity Formulation

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