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Clinical Trials/CTRI/2023/02/049401
CTRI/2023/02/049401RecruitingPhase 4

A double blind, randomized, placebo controlled clinical study to Evaluate the efficacy of Cannasen Nasal spray Night in patients with insomnia

Cannordic A/S0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 4
Status
Recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Pms

Eligibility Criteria

Inclusion Criteria

  • 1. Patient from 18 to 65 years of age.
  • 2. Patient with the history of seasonal pollen allergy.
  • 3. If female with childbearing potential, must be willing to practice an acceptable form of birth control for the duration of the study.
  • 4. Patient that are able to give written informed consent in a manner approved by the institutional ethics committee and comply with the requirements of the study.
  • 5. Patient willing to avoid participation in any other interventional clinical trial for the duration of the study.

Exclusion Criteria

  • 1. Females that are pregnant, breast feeding, or planning to get pregnant during the study.
  • 2. Patient that have participated in any other interventional clinical trial in the previous 30 days.
  • 3. Patient with known sensitivity to any of the constituents of the investigational product.
  • 4. Patient that are taking applying other product.

Investigators

Sponsor
Cannordic A/S

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