Benign Prostatic Hyperplasia. Hyperplasia of prostate
Conditions
Interventions
Intervention 1: First intervention group: Patients receiving a single 50 microgram dose of neostigmine (with the chemical composition of neostigmine methyl sulfate and 0.5 mg per ml, Caspian Tamin Pha
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: All patients who are candidates for TURP and who are referred to Amir al-Momenin and Valiasr hospitals in Arak as elective procedures Patients in the age range of 30-70 years All patients with ASA class 1 and 2 Absence of heart, lung and liver diseases BMI less than or equal to 35 All TURP candidates undergoing spinal anesthesia Insensitivity to neostigmine, sufentanil and magnesium sulfate Maximum duration of surgery less than or equal to 90 minutes
Exclusion criteria
Exclusion criteria: All patients in whom spinal anesthesia fails for any reason and we have to resort to general anesthesia All patients whose surgery lasts more than 90 minutes Patients outside the age range of 30-70 All patients who experience cardiac and respiratory arrest during surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average pain score in three groups. Timepoint: Recovery, 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Visual Analog Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Shivering. Timepoint: Recovery. Method of measurement: Checklist; Binary Shivering asssessment.;Nausea and vomiting. Timepoint: Recovery. Method of measurement: Checklist; Binary Nausea and vomiting assessment.;Mean arterial pressure. Timepoint: Recovery. Method of measurement: Standard monitoring of vital signs in the operating room and recovery room.;Average heart rate. Timepoint: Recovery. Method of measurement: Standard operating room and recovery room cardiac monitoring and electrocardiogram.;Average of peripheral oxygen saturation. Timepoint: Recovery. Method of measurement: Pulse oximetry.;Average narcotic usage. Timepoint: 24 hours after surgery. Method of measurement: Medication registration checklist and patient file.;Average duration of pain relief. Timepoint: After surgery. Method of measurement: Recording the time of the patient's first request for narcotic and the patient's file. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Rasoul Jafari
Arak University of Medical Sciences
Outcome results
None listed