medical surveillance following treatment. Follow-up examination after surgery for other conditions
Conditions
Interventions
Intervention 1: In the first group patients in the same way with propofol 2 mg / kg and midazolam 0.01 mg / kg and sufentanil 0.2 mg / kg and neuromuscular 0,5 mg / kg will put under general anesthesi
Treatment - Drugs
In the first group patients in the same way with propofol 2 mg / kg and midazolam 0.01 mg / kg and sufentanil 0.2 mg / kg and neuromuscular 0,5 mg / kg will put under general anesthesia. Isoflurane ga
In the second group patients in the same way with propofol 2 mg / kg and midazolam 0.01 mg / kg and sufentanil 0.2 mg / kg and neuromuscular 0,5 mg / kg will put under general anesthesia. Isoflurane g
In the third group patients in the same way with propofol 2 mg / kg and midazolam 0.01 mg / kg and sufentanil 0.2 mg / kg and neuromuscular 0,5 mg / kg will put under general anesthesia. Isoflurane ga
In the forth group patients in the same way with propofol 2 mg / kg and midazolam 0.01 mg / kg and sufentanil 0.2 mg / kg and neuromuscular 0,5 mg / kg will put under general anesthesia. Isoflurane ga
In the control group do not use the gel and intubation performed as usual.The patients for the occurrence of straining and cough and laryngospasm and bronchospasm will control by a person who is unawa
Sponsors
Vice chancellor for research, Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: age between 20 and 60 years; patient informed consent;patients admitted for cholecystectomy laparoscopic surgery; ASA class 1,2; mallampati 1 or 2; TMD >6cm. Exclusion criteria: history of smoking or drug abuse;a history of catching a cold in the last two weeks; patients with COPD, asthma and convulsions.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sore throat. Timepoint: 1 and 6 and 12 hourse after extubation. Method of measurement: VAS.;Coughing. Timepoint: Immediately aftr extubation. Method of measurement: By asking of patient.;Straining. Timepoint: extubation time. Method of measurement: By asking of patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| Laryngospasm. Timepoint: after extubation. Method of measurement: exist - lack.;Bronchospasm. Timepoint: after extubation. Method of measurement: exist - lack. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Rahmatinejad
kermanshah univrsity of medical science
Outcome results
None listed