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Individualized Homeopathic Medicines in Stage I Essential Hypertension: A Double-Blind, Randomized, Placebo-Controlled Pilot Trial.
Sadhukhan, Satarupa; Singh, Subhas; Michael, James; Misra, Pankhuri; Parewa, Maneet; Nath, Arunava; Magotra, Nitin; Kundu, Nivedita; Basu, Anamika; Ali, Sk Swaif; Koley, Munmun; Saha, Subhranil.
Affiliation
  • Sadhukhan S; Department of Organon of Medicine and Homoeopathic Philosophy, National Institute of Homoeopathy, Kolkata, India.
  • Singh S; Director, National Institute of Homoeopathy, Kolkata, India.
  • Michael J; Department of Organon of Medicine and Homoeopathic Philosophy, National Institute of Homoeopathy, Kolkata, India.
  • Misra P; Department of Materia Medica, National Institute of Homoeopathy, Kolkata, India.
  • Parewa M; Department of Repertory, National Institute of Homoeopathy, Kolkata, India.
  • Nath A; Department of Organon of Medicine and Homoeopathic Philosophy, National Institute of Homoeopathy, Kolkata, India.
  • Magotra N; Department of Organon of Medicine and Homoeopathic Philosophy, National Institute of Homoeopathy, Kolkata, India.
  • Kundu N; Department of Organon of Medicine and Homoeopathic Philosophy, National Institute of Homoeopathy, Kolkata, India.
  • Basu A; Department of Practice of Medicine, Mahesh Bhattacharyya Homoeopathic Medical College and Hospital, Government of West Bengal, Howrah, India.
  • Ali SS; Department of Practice of Medicine, Mahesh Bhattacharyya Homoeopathic Medical College and Hospital, Government of West Bengal, Howrah, India.
  • Koley M; Department of Organon of Medicine and Homoeopathic Philosophy, State National Homoeopathic Medical College and Hospital, Government of Uttar Pradesh, Lucknow, India.
  • Saha S; Department of Repertory, D. N. De Homoeopathic Medical College and Hospital, Government of West Bengal, Kolkata, India.
J Altern Complement Med ; 27(6): 515-521, 2021 Jun.
Article in En | MEDLINE | ID: mdl-33760643
ABSTRACT

Objective:

The present study assessed the feasibility of a definitive placebo-controlled trial for evaluating individualized homeopathy (IH) in stage I hypertension (HTN).

Design:

Double-blind, randomized (IH 34, placebo 34), placebo-controlled, parallel arms, pilot trial. Settings/Location National Institute of Homoeopathy, India.

Subjects:

Patients suffering from stage I HTN.

Interventions:

IH and identical-looking placebo. Outcome

measures:

Feasibility issues, blood pressure (BP) and Measure Yourself Medical Outcome Profile-2 (MYMOP-2) were assessed for 6 months.

Results:

The recruitment and retention rates were 44.4% and 85.3%, respectively. Group differences were seemingly higher in the IH group than in the placebo group.

Conclusions:

Despite challenges in recruitment, an adequately powered efficacy trial appears feasible in the future.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Materia Medica / Essential Hypertension Type of study: Clinical_trials Limits: Humans Country/Region as subject: Asia Language: En Journal: J Altern Complement Med Journal subject: TERAPIAS COMPLEMENTARES Year: 2021 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Materia Medica / Essential Hypertension Type of study: Clinical_trials Limits: Humans Country/Region as subject: Asia Language: En Journal: J Altern Complement Med Journal subject: TERAPIAS COMPLEMENTARES Year: 2021 Document type: Article Affiliation country: India