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Recruiting Early Phase 1

Effect of Preoperative Oral Pregabalin Versus Intraoperative Fentanyl on Postoperative Analgesia

NCT05150795 · tracked via the Priya Life Science Egypt tracker
Phase
Early Phase 1
Started
2022-01-01
Last updated
2025-01-29

Condition(s) studied

Post Operative Pain, Acute

Investigational drug(s) / intervention(s)

Pregabalin 150mg →Fentanyl 100 micrograms ampoule

Pregabalin 150mg: Compare the postoperative analgesic effect of pre-operative oral pregabalin (Study group), to the intraoperative intravenous fentanyl (Control group) in diagnostic laparoscopic gynecologic surgery.

Fentanyl 100 micrograms ampoule: Compare the postoperative analgesic effect of pre-operative oral pregabalin (Study group), to the intraoperative intravenous fentanyl (Control group) in diagnostic laparoscopic gynecologic surgery.

Study summary

Pregabalin is a structural analogue of gamma amino butyric acid (GABA). It binds to presynaptic alpha-2-delta subunit of voltage gated calcium channels in the brain and the spinal cord. Thus, it modulates the release of excitatory neurotransmitters, such as glutamate, norepinephrine, substance-P, and calcitonin gene related peptide. Also, it causes inhibitory modulation of overexcited neurons and restores them to a normal state.

Pre-emptive analgesia aims to reduce postoperative opioid consumption especially in ambulatory surgeries. Pregabalin (PGB) is an emerging drug in this field. Different doses of preoperative oral pregabalin (75, 150 and 300 mg) are described in the literature with a dose-response analgesic relationship and reduction of opioid use; however increasing the dose results in increasing the incidence of side effects mainly sedation and dizziness.

Perioperative use of opioids for analgesia may result in side effects; like nausea, vomiting, excessive sedation, respiratory depression, pruritus, and urinary retention.The concomitant use of opioids with pregabalin may result in excess sedation and somnolence, so, the use of opioids with pregabalin should be limited to patients with inadequate alternative options.

Eligibility

Sex
FEMALE
Min age
21 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * ASA physical status I Exclusion Criteria: * Patients' refusal * use of sedatives, hypnotics, anti-psychotic or antidepressant drugs * history of drug/alcohol abuse * history of chronic pain * daily intake of analgesics * history of epilepsy

Primary outcome measure(s)

  • Changes in post-operative pain score at rest over time — 1 hour
    Intensity of pain will be monitored at 15 and 30min after arrival to the PACU, then 1h before discharge from the PACU. For analysis, pain severity will be categorized as absent (VAS=0), mild (VAS=1-3), moderate (VAS=4-7), severe (VAS=7-9), and very severe (VAS=10).
  • Changes in post-operative pain score on coughing over time — 1 hour
    Intensity of pain will be monitored at 15 and 30min after arrival to the PACU, then 1h before discharge from the PACU. For analysis, pain severity will be categorized as absent (VAS=0), mild (VAS=1-3), moderate (VAS=4-7), severe (VAS=7-9), and very severe (VAS=10).

Trial sites (1)

FacilityCityRegionStatus
Ain-Shams University Cairo Egypt Recruiting
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 NCT05150795 on ClinicalTrials.gov ↗ ← All trials in Egypt