Anaesthesia
Conditions
Interventions
Opoid based anesthesia
Sponsors
Mansoura University Hospitals
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women aged between 40 to 70 years American Society of Anesthesiologists physical status (ASA) I & II undergoing scheduled laparoscopic hysterectomy
Exclusion criteria
Exclusion criteria: patients refusal, body mass index >35 kg m- 2, hepatic, renal and cardiac insufficiency, DM history of chronic pain, psychiatric disease, allergy, contraindication to any of the study drugs, inability to assess pain.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main result of this research (primary outcome) will be the visual analogue scale (VAS) on the first postoperative day in the PACU and ward, including the highest VAS pain levels within the 2, 6, 12, 24 and 48 h following surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome indicators for this study include the total amount of fentanyl, dexmedetomidine, and propofol used during the procedure, as well as hemodynamic data such as the profile of MAP, HR, and SpO2 at various measurement times (before induction, after induction, immediately after tracheal intubation, after artificial pneumoperitoneum, at cessation of anesthetics and immediately after extubation). Additionally, postoperative opioid-related adverse events will be recorded. | — |
Countries
Egypt
Contacts
Public ContactMohamed Albayomy
Resident
Outcome results
None listed