Improving Sleep Quality & Perception of Change: over skin application of Magnesium for Adults with Neck Pai

Phase 3

• Conditions: Health Condition 1: M999- Biomechanical lesion, unspecified

• Registration Number: CTRI/2024/03/064936
• Lead Sponsor: Galgotias University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Persistent Neck Pain duration more than 3 months.

2. Health Status: Individuals without diagnosed medical conditions affecting magnesium metabolism or utilization.

3. Ability to Provide Informed Consent: Participants must be capable of understanding the study procedures and providing informed consent.

4. Availability: Participants must be available for the duration of the study and willing to adhere to the intervention protocol.

Exclusion Criteria

1. Known Magnesium Deficiency: Individuals with diagnosed magnesium deficiency or receiving magnesium supplementation at the time of enrollment.

2. Chronic Medical Conditions: Participants with chronic medical conditions (e.g., renal disease, gastrointestinal disorders) known to affect magnesium absorption or metabolism.

3. Medication Use: Individuals currently taking medications known to interfere with magnesium absorption or metabolism (e.g., proton pump inhibitors, diuretics).

4. Pregnancy or Lactation: Pregnant or lactating individuals, as magnesium requirements may differ during these periods.

5. Allergy or Sensitivity: Individuals with known allergies or sensitivities to magnesium or any components of the supplementation product (e.g., Spray 10 spray).

6. Participation in Other Clinical Trials: Participants currently enrolled in or have participated in other clinical trials within a specified timeframe prior to enrollment.

7. Inability to Comply: Individuals unable or unwilling to adhere to the study protocol, including attending scheduled assessments and following supplementation instructions.

Study & Design

• Study Type: Interventional
• Study Design: Not specified