Skip to main content
Clinical Trials/CTRI/2021/07/034849
CTRI/2021/07/034849
Completed
未知

A single blind randomized clinical study comparing Mu?kak ?di ga?a ghanava?i and Navakaguggulu along with lifestyle modification in Sthaulya (Obesity) - Obesity

J S Ayurveda College and P D Patel Ayurveda hospital NADIAD0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
J S Ayurveda College and P D Patel Ayurveda hospital NADIAD
Enrollment
100
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
J S Ayurveda College and P D Patel Ayurveda hospital NADIAD

Eligibility Criteria

Inclusion Criteria

  • 1\. Patient fulfilling the above criteria of diagnosis for Sthaulya (Obesity)

Exclusion Criteria

  • 1\. Patient having endocrinal diseases e.g Hypothyrosim, Cushing’s syndrome, Acromegaly, etc 2\. Drug\-induced obesity e.g patients taking antidepressants, corticosteroids, hypnotics, etc.
  • 3\. Patient having gynecological diseases e.g. PCOD, PCOS, etc
  • 4\. Patient having a systemic illness like Tuberculosis, Carcinoma, Hypertension, Diabetes mellitus, Coronary artery diseases, major Renal or Liver disorder, etc
  • 5\. Pregnant and lactating women

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Phase 4
A study comparing two brands of similar suture materials (Trulon�® and Ethilon�® polyamide suture), for closure of the skin following open abdominal surgeriesHealth Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: N859- Noninflammatory disorder of uterus, unspecified
CTRI/2020/09/027978Healthium Medtech Pvt Ltd104
Completed
Phase 4
A clinical trial to compare tissue reaction/inflammation with Trusilk�® (Healthium) and Mersilk�® (Johnson & Johnson) silk sutures post primary closure of mucosa in subjects undergoing planned surgical removal of impacted mandibular third molar at 72 hours and 7 days.Health Condition 1: O- Medical and Surgical
CTRI/2020/03/024100Healthium Medtech PvtLtd formerly Sutures India Pvt Ltd132
Completed
Phase 4
Clinical equivalence study of two polydioxanone sutures (PD Synth and PDS) for abdominal fascial closure following midline laparotomy
CTRI/2020/04/024955Healthium Medtech PvtLtd formerly Sutures India Pvt Ltd96
Completed
Phase 4
A comparative clinical equivalence study of Trulene® and Prolene® polypropylene mesh in patients undergoing Lichtenstein open repair of primary inguinal hernia secured with sutures at 6 and 12 months
CTRI/2020/02/023307Healthium Medtech PvtLtd formerly Sutures India Pvt Ltd132
Completed
Phase 4
A clinical equivalence study of two polypropylene sutures (Trulene and Prolene) in elective primary coronary artery bypass graft surgeryHealth Condition 1: O- Medical and Surgical
CTRI/2020/05/025157Healthium Medtech Pvt Ltd formerly Sutures India Pvt Ltd92