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Postspinal Headache and Near Infrared Spectroscopy (NIRS)

H

Hakan Tapar

Status

Unknown

Conditions

Tissue Oxygenation

Study type

Observational

Funder types

Other

Identifiers

NCT04187846
18-KAEK-167

Details and patient eligibility

About

Evaluation of the relationship between postspinal headache and near infrared spectroscopy in cesarean section patients

Full description

Patients with cesarean section under spinal anesthesia were included in the study. Before the study, patients were moniterized with NIRS device in the preoperative waiting room.NIRS moniterization was continued intraoperatively at 1st, 4th, 7th, 10th, 15th, 30th minutes and 24th postoperative period.

Patients were divided into two groups as those with postspinal headache (Group A) and those with postspinal headache (Group B). In this study, NIRS values between two groups were compared.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective cesarean section

Exclusion criteria

  • Not willing to participate in the study
  • Use of anti-psychotic or anti-depressant drugs
  • Patients with headaches

Trial contacts and locations

1

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Central trial contact

Hakan Tapar

Data sourced from clinicaltrials.gov

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