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Clinical Trials/IRCT20130416013027N2
IRCT20130416013027N2
Recruiting
Phase 1

The survey of transcranial direct current stimulation efficacy on the post-traumatic sleep quality, insomnia severity in the patients with mild traumatic brain injury during sub-acute phase

Rasht University of Medical Sciences0 sites64 target enrollmentTBD
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Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Rasht University of Medical Sciences
Enrollment
64
Status
Recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Rasht University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •patients aged 18 to 65 years
  • •Normal and abnormal findings on brain scans within the first 24 hours of hospitalization
  • •all TBI severity
  • •at least 2 weeks to one month after the time of injury onset
  • •The ISI score is over 7 .

Exclusion Criteria

  • •People with a history of primary sleep disorders
  • •taking psychotropic drugs one month before entering the study
  • •having serious neurological and psychiatric disorders
  • •patients with previous traumas
  • •those with tDCS contraception, such as pregnant patients, patients with metal implants or pains, those having a heart pacemaker, taking a psychoactive drug or an effective CNS drug, substance abusers, existence of psychiatric and neurological diseases , a history of seizure, epilepsy, tumor, Neurotrauma, stroke, or neurological diseases, those experiencing skin eczema under the tDCS electrodes
  • •Clinical instability or having behavioral problems that prevent the cooperation of the subject in the intervention
  • •The use of sodium and calcium\-dependent calcium channel blockers such as phenytoin, carbamazepine, verapamil, nimesadine, and flonarazine
  • •having a serious complication associated with tDCS
  • •The patient's dissatisfaction with the continuation of the study

Outcomes

Primary Outcomes

Not specified

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