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Clinical Trials in Egypt / NCT07800364
Recruiting Not applicable

The Effect of Preoperative Administration of Oral Tizanidine on the Postoperative Pain and Sleep Quality

NCT07800364 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-03-01
Last updated
2026-09-02

Condition(s) studied

The Effect of Preoperative Administration of Oral TizanidinePost Operative Pain

Investigational drug(s) / intervention(s)

TizanidinePlacebo

Tizanidine: oral administered preoperatively

Placebo: oral placebo adminstered preoperatively

Study summary

The majority of lower limb fractures treated with surgery often leading to significant morbidity and mortality. Despite improvements in perioperative care, about 20% suffer from severe postoperative complications. So, effective perioperative pain management is crucial in this demographic to ensure optimal recovery and reduce complications. (1) Controlling the postoperative pain often begins in recovery room by using opioids, especially morphine. However, systemic opioids may develop many complications such as nausea and vomiting, apnea, respiratory depression, and urinary retention. To reduce the complications and consumption of the opioids, other procedures are recommended. One of these procedures is preemptive analgesia(2).

In addition to pain, disrupted sleep quality is a common challenge, with evidence suggesting a bidirectional relationship where poor sleep exacerbates pain, and pain further disrupts sleep (3). Addressing both pain and sleep disturbances in the perioperative period is therefore critical for enhancing recovery and improving overall patient outcomes

Eligibility

Sex
ALL
Min age
21 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged ≥ 21 years * Scheduled for lower limb orthopedic surgery * Able to provide informed consent Exclusion Criteria: * History of hypersensitivity to tizanidine * Pregnancy or breastfeeding * Failure of spinal anesthesia or inadequate block.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
tanta University hospital Tanta Gharbia Governorate Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07800364 on ClinicalTrials.gov ↗ ← All trials in Egypt