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Scalp acupuncture and primary hypertension

Effect of scalp acupuncture in primary hypertension:A randomized controlled trial. - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060555
Enrollment
60
Registered
2023-12-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: I10- Essential (primary) hypertension

Interventions

Intervention1: Scalp acupuncture: The sterile Copper handled single use needles will be inserted at vasomotor area in the scalp acupuncture therapy, 3 sittings per week on the alternate days for
30 MINS Needle
Copper handled sterile,single use needles of length 1-2 Cun, Diameter
28- 30 guage will be used. Control Intervention1: No intervention: Patients will be under observation and after completion of the study the control group will be recieving scalp acupuncture for

Sponsors

Dr Veni S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ?Age between 40 to 60 years of both male and female gender ?Patients with history of 1 to 5 years of Grade 1Primary Hypertension ?Patients under single drug or 2 drug combination of Thiazide / Thiazide like diuretics, Calcium channel blockers,Angiotensin converting enzyme inhibitors and other blood thinning drugs in minimum half to maximum dosage ?Clinically stable patients ?All subjects gave their informed consent,

Exclusion criteria

Exclusion criteria: ? Comorbidities that would prohibit participation in study procedures, including active renal dialysis, metastic cancer ? Scar in the scalp needling area ? Enrollment in other studies that involved active interventions; ? Psychiatric comorbidities & Needle phobia Patients with secondary hypertension

Design outcomes

Primary

MeasureTime frame
Assessment of Blood pressure in primary hypertensive patients is done using arm type non invasive digital blood pressure monitoring apparatus. Outcome measures will be measured, at the end of the 6th week( end of the intervention )Timepoint: 3 sittings per week on the alternate days for 6 weeks

Secondary

MeasureTime frame
No secondary outcome is included in this studyTimepoint: Not Applicable

Countries

India

Contacts

Public ContactDr.N.Prabhu

international institute of yoga and naturopathy medical sciences

drprabubnys91@gmail.com9566351891

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026