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effect of administration of intrathecal Dexmedetomidine on the Spinal Cord Mori

Evaluating the effect of administration of intrathecal Dexmedetomidine on the Spinal Cord Mori levels of apoptotic factors in patients scheduled for lumbar disc surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200127046282N1
Enrollment
40
Registered
2020-04-19
Start date
2019-12-22
Completion date
Unknown
Last updated
2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar disc herniation. Thoracic, thoracolumbar, and lumbosacral intervertebral disc disorders

Interventions

Intervention 1: Intervention group: After surgical incision a spinal cord fluid sample of 1 cc is taken from the site of surgery, the needle stays in place and the syringe is removed and with another

Sponsors

Vice chancellor for research, Shahid Beheshti University of Medical Sciences , Loghman Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: No history of taking anti-inflammatory drugs two weeks before surgery Lack of AIDS and immunosuppressive diseases

Exclusion criteria

Exclusion criteria: GCS reduction for a reason other than stroke Change in the type of surgery according to the surgeon's opinion History of systemic diseases such as diabetes mellitus, renal failure and chronic pulmonary heart disease

Design outcomes

Primary

MeasureTime frame
The level of Bax / Bcl-2¬ apoptotic factor in cerebrospinal fluid in dexmedetomidine and placebo group. Timepoint: After surgery and at the end of surgery. Method of measurement: Study of cerebrospinal fluid in dexmedetomidine and placebo group by ELISA.;Numering Rating Scale (NRS) Pain score in dexmedetomidine and placebo group. Timepoint: Before anesthesia and in recovery. Method of measurement: NRS scoring system.;The level of caspase-3 apoptotic factor in cerebrospinal fluid in dexmedetomidine and placebo group. Timepoint: After surgery and at the end of surgery. Method of measurement: Study of cerebrospinal fluid in dexmedetomidine and placebo group by ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Sam Hosseininasab

Shahid Beheshti University of Medical Sciences

sam.hn617@gmail.com+98 21 2221 5558

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026