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Effect of neutral spinal spray on hypertensio

Phase 1
Conditions
Health Condition 1: I10- Essential (primary) hypertension
Registration Number
CTRI/2024/04/065869
Lead Sponsor
Dr Smriti Goswami
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Pre-diagnosed primary hypertensive subjects

2. Either on or not on regular medication

3. Subjects who are willing to participate after signing the informed consent form

Exclusion Criteria

1. Subjects using any psychoactive substances, sedatives, anxiolytics, anti-depressants, and consuming alcohol and nicotine

2. Pyrexia due to any reason

3. Diabetic Neuropathy

4. Mental illnesses

5. Subject with open wound

6. Pregnant Women

7. Female subjects during the menstrual cycle because autonomic variables vary during this period

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Heart Rate Variability (HRV)Timepoint: Pre and post intervention
Secondary Outcome Measures
NameTimeMethod
Blood Pressure (SBP, DBP), Pulse Rate, Heart Rate.Timepoint: Pre & post intervention
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