About this trial
Effect of spinal anesthesia with bupivacaine versus prilocaine on postoperative shivering after inguinal hernia repair : a prospective randomized double blind study
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
patients with inguinal hernia under spinal anesthesia aged from 20 to 60 years
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Bupivacaine Spinal Anesthesia
DrugGroup B: (n=40) patients receiving hyperbaric bupivacaine 0.5% (Marcaine, Sunny Medical, Egypt).
Prilocaine spinal anesthesia
DrugGroup P; (n=40) will receive prilocaine2% (Takipril, Sunny Medical, Egypt).
Spinal Anesthesia (bupivacaine) spinal anesthsia (prilocaine)
DrugIn both groups the patients will be in the sitting position after preparation and draping of the patient's back. A skin wheal will be made by 1 ml of lidocaine HCl 2% at L3-4 interspace using a 25-gauge needle. Hyperbaric bupivacaine 0.5% will be given in dose (15mg) in group B and hyperbaric prilocaine2% in dose (60mg) in Group P. Anesthesia will be prepared by personnel not involved in this study. Patients will be supplemented with oxygen 5.0 l/minute by face mask. Time to achieve T10 dermatome will be recorded also motor level by modified Bromage motor blockade score; 4=no motor block, 3=can flex leg at knee, 2=can flex leg at the ankle and 1= complete motor block. The time needed to reach the maximum block will be recorded. In both groups the hemodynamic parameters will be recorded before block, immediately after block then every 5 min till end of the operation. Need for sedation or analgesia will be recorded.
Treatment groups
Trial outcomes
Primary outcomes
shivering using bedside shivering assesement score ( BSAS)
shivering using bedside shivering assesement score ( BSAS)
shivering using bedside shivering assesement score ( BSAS)
Locations
Sponsors and contacts
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Amr mohamed
Lead sponsor
Theodor Bilharz Research Institute
Sponsor institution
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