Skip to main content
Clinical Trials/SLCTR/2021/021
SLCTR/2021/021RecruitingPhase 2

A single-center, randomized, six month, parallel-group, study to compare the effectiveness of a combination of physiotherapy and Ayurveda treatment versus physiotherapy and placebo in ischemic stroke rehabilitation.

Higher degree, Research and Publication Committee0 sitesStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • Patients confirmed to have an ischemic stroke
  • Patients above 18 years of age
  • * Both men and women
  • Barthel Index 0-50 (severely disabled patients)
  • NIHSS score (The National Institutes of Health Stroke Scale Score) 5-20 on admission.
  • Non- thrombolysis patients

Exclusion Criteria

  • Stroke mimics (A nonvascular disease that presents with stroke-like symptoms, often indistinguishable from an actual stroke)
  • Eg: brain tumors (gliomas, meningiomas, adenomas)
  • * Toxic/ metabolic disorders ( hypoglycemia, hypercalcemia, hyponatremia, uremia, hepatic encephalopathy, hyperthyroidism, thyroid storm)
  • * Infectious disorders (meningio encephalitis)
  • * Psychological disorders
  • * Migraines
  • * Seizures
  • * Demyelination disorders
  • Posterior circulation stroke
  • Hemorrhagic strokes
  • Patients without a caregiver, relative or a supporting family

Investigators

Sponsor
Higher degree, Research and Publication Committee

Similar Trials

Active, not recruiting
Not Applicable
A 6 months, multicenter study to evaluate the effect of an individualized patient support program on treatment satisfaction in Fingolimod (FTY720)-treated patients with relapsing-remitting multiple sclerosisTreatment statisfaction in patients with relapsing remitting Multiple SclerosisMedDRA version: 15.0Level: PTClassification code 10063399Term: Relapsing-remitting multiple sclerosisSystem Organ Class: 10029205 - Nervous system disorders
EUCTR2012-002637-11-DEovartis Pharma GmbH
Completed
Not Applicable
Changes in Resting Energy Expenditure with Two Different Schedules of Calorie RestrictioObesity
ACTRN12617000635369Assoc Prof Jeremy Krebs36
Active, not recruiting
Not Applicable
A 6-month, multicenter, randomized, controlled parallel group study to evaluate the effect of physical training on fatigue in patients with relapsing-remitting multiple sclerosis treated with fingolimod (Gilenya®), followed by a 6 month optional extension phase
EUCTR2011-002969-38-DEovartis Pharma GmbH
Active, not recruiting
Phase 1
Combination treatment with dapagliflozin and exenatide to investigate the effect of weight loss in subjects with obesity compared to placebo.Obesity defined as body mass index (BMI) 30-45 kg/m2Obesity related metabolic disordersMedDRA version: 18.0Level: LLTClassification code 10029885Term: Obesity, unspecifiedSystem Organ Class: 100000004861
EUCTR2014-003432-39-SEDept of Medical Sciences, Clinical Diabetes and Metabolism, Uppsala University
Completed
Phase 3
BE study of Budesonide 80 µg and Formoterol Fumarate Dihydrate 4.5 µg inhalation product in asthma patient
CTRI/2022/08/044640Cipla Ltd1,191