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Clinical Trials/CTRI/2023/03/050878
CTRI/2023/03/050878
Recruiting
N/A

A prospective interventional study to assess role of an integrated approach of Homoeopathy along with WHO Rehabilitation self-management care for long COVID: Single blind placebo controlled randomized trial

Central Council for Research in Homoeopathy0 sites0 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Health Condition 1: U071- COVID 19 virus identified
Sponsor
Central Council for Research in Homoeopathy
Status
Recruiting
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
Central Council for Research in Homoeopathy

Eligibility Criteria

Inclusion Criteria

  • History of confirmed COVID\-19 infection in last 6 months; Minimum 4 weeks after the confirmed COVID\-19 report.
  • Residual or any other clinical complaints reported to be occurring after COVID\-19 like fatigue, fever (unknown reason), anxiety, joint pain, breathlessness, headache, or any other non\-serious clinical illness not explained by an alternative diagnosis.
  • Cases who have recovered clinically\&/or laboratory confirmed negative.
  • Patients agreeing to perform WHO self\-care rehabilitation program under guidance of the physician.
  • Patients willing to participate in the study and give written informed consent

Exclusion Criteria

  • Patients having any serious sequelae, presence of systemic complications (persistent organic damage) or specific organ dysfunction due to SARS\-CoV\-2 virus.
  • Uncontrolled cases of DM, HT, Asthma, HIV, active TB, Cancer, immune compromised illness like HIV etc.
  • Patients having severe dyspnoea with Oxygen saturation below 95%; patients requiring ventilation support
  • Patient reporting having Psychiatric disorders, hepatic and renal dysfunction.
  • Contra indications to physical exercise or Patient unable to do exercise in the WHO rehabilitation self\-management care plan.
  • Patients not able to give written informed consent

Outcomes

Primary Outcomes

Not specified

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