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Evaluation of the Impact of the HL Natural, Inc. Tension Relief Product

NCT04091555 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 117

Last updated 2021-11-15

No results posted yet for this study

Summary

The primary hypothesis of the present study is that supplementation with the Tension Relief test product will reduce the severity of symptoms of a tension headache.

Conditions

Interventions

DIETARY_SUPPLEMENT

HLNatural Tension

Understand the impact of the supplement on Tension Headaches

Sponsors & Collaborators

  • HLNatural, Inc.

    collaborator INDUSTRY

  • Hawthorne Effect Inc.

    lead OTHER

Principal Investigators

  • Soyona Rafatjah, MD · Hawthorne Effect Inc.

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-16
Primary Completion
2020-08-16
Completion
2020-09-16

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04091555 on ClinicalTrials.gov