Comparative Study of Hemodynamic Changes Caused by Diazepam and Midazolam During Third Molar Surgery
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|ClinicalTrials.gov Identifier: NCT02177955|
Recruitment Status : Completed
First Posted : June 30, 2014
Last Update Posted : June 30, 2014
Objective: The aim of the present study was to compare hemodynamic changes using 7.5 mg of midazolam and 10.0 mg of diazepam during the surgical removal of symmetrically positioned third molars.
Study design: A prospective, randomized, double-blind, clinical trial was carried out involving 120 patients divided in three groups: Group 1 (diazepam and placebo), Group 2 (midazolam and placebo) and Group 3 (diazepam and midazolam). Each subject underwent two surgeries on separate occasions under local anesthesia.
|Condition or disease||Intervention/treatment||Phase|
|Anxiety||Drug: 7.5 mg Midazolam Drug: 10 mg diazepam||Phase 4|
Study design A double-blind, randomized, crossover, clinical trial with a split-mouth design was carried out. This study received approval from the Human Research Ethics Committee of the institution at which it was carried out (process number: 001.0.097.000-08) and was conducted in compliance with the Consolidated Standards of Reporting Trials (CONSORT) statement. All patients signed a statement of informed consent agreeing to participate in the study.
Sample size and pilot study The sample size was estimated using the a computational program. Thirty patients were submitted to third molar surgeries in a pilot study to determine the sample size. This step was necessary due to the lack of similar studies in the literature. Calculations were performed with specific programs taking into consideration the variables, a 95% confidence interval, 80% test power and 5% error. At the end of the study, 120 patients were analyzed (40 in each group), totaling 240 surgeries.
Sample selection One hundred twenty eight individuals between 18 and 40 years of age were selected for participation in the present study and submission to maxillary and mandibular third molar extractions bilaterally at the Department of Oral-Maxillofacial Surgery. Each patient was to be submitted to two surgeries. The third molars (maxillary or mandibular) needed to have the same degree of impaction on both sides.
Three groups were formed: Group A received diazepam and placebo, Group B received midazolam and placebo and Group C received midazolam and diazepam. For the purposes of randomization and blinding of the surgeon and researcher in charge of analyzing the results, the groups were renominated Groups 1, 2 and 3. The randomization procedure was carried out by a researcher who was not directly involved in the surgeries or evaluations. Sequentially numbered, sealed, opaque envelopes were used, each containing a combination of substances and the side to be submitted to the first surgery. For each patient, the researcher opened an envelope, informed the main investigator and surgeon of the side to be operated, and administered the substance to the patient. The second surgery was performed on the contralateral side with the administration of the second substance. Blinding was performed to avoid awareness regarding what substance was administered in each surgery. For such, the pills were fabricated with the same outer color and a standardized size at the Pernambuco Pharmaceutical Laboratory (Brazil) and were packaged in recipients with the same color. The recipients were denominated 1, 2 and 3.
Surgical procedures and medications As the patients were classified as healthy, no prophylactic use of antibiotics was performed prior to surgery for the prevention of bacterial endocarditis, as recommended by the American Heart Association. All patients rinsed their mouths with 0.12% chlorhexidine for one minute prior to surgery to reduce the bacterial population in the oral cavity. Moreover, all patients were instructed to take two 4-mg pills of dexamethasone one hour prior to surgery. The use of a corticosteroid in the preoperative period minimizes the occurrence of postoperative swelling and reduces the risk of trismus.13 The substances (diazepam, midazolam and placebo) were administered orally 45 minutes prior to the surgical procedure. As the substances were masked, neither the surgeon nor the patient was aware of what substance was given (double-blind study).
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||120 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||Comparative Study of Hemodynamic Changes Caused by Diazepam and Midazolam During Third Molar Surgery. A Prospective Randomized Study|
|Study Start Date :||January 2011|
|Actual Primary Completion Date :||July 2012|
|Actual Study Completion Date :||September 2012|
Placebo Comparator: midazolan
7.5 mg midazolan 45 minutes before the surgery
Drug: 7.5 mg Midazolam
7.5 mg midazolam 45 minutes before surgery
Placebo Comparator: diazepam
10 mg diazepam 45 minutes before the surgery
Drug: 10 mg diazepam
10 mg midazolam 45 minutes before surgery
- Changes from baseline in systolic blood pressure until the end of surgery [ Time Frame: baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery. ]
- Changes from baseline in diastolic blood pressure until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]
- Changes from baseline in mean blood pressure until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]
- Changes from baseline in heart rate until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]
- Changes from baseline in rate pressure product until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]The rate pressure is the product of the multiplication of systolic blood pressure by heart rate
- Changes from baseline in oxygen saturation until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]
- Change from baseline in pressure rate quotient until the end of surgery [ Time Frame: Baseline, 2 minutes, 7 minutes, 12 minutes, end of surgery ]Pressure rate quotient is calculated by dividing mean blood pressure by heart rate
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02177955
|School of Dentistry of Pernambuco|
|Recife, Pernambuco, Brazil, 54756220|
|Principal Investigator:||Hécio H De Morais, PhD||University of Pernambuco|