The Effect of Premedication Methods to be Applied to Prevent Preoperative Anxiety in Patients Who Will be Operated for Breast Cancer, on Postoperative Anxiety and Pain
Overview
- Phase
- Not Applicable
- Intervention
- Precedex and dormicum
- Conditions
- Female Patients Under the Age of 65 Who Will Undergo Breast Cancer Surgery
- Sponsor
- Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- effect of premedication on postoperative pain and anxiety scores
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
In this study, it was investigated whether the premedication drug administered before the surgery had an effect on postoperative pain and anxiety scores in female patients under the age of 65 who will undergo breast cancer surgery.
Detailed Description
In this study, it was investigated whether the premedication drug administered before the surgery had an effect on postoperative pain and anxiety scores in female patients under the age of 65 who will undergo breast cancer surgery. The STAI-1(State Trait Anxiety İnventory ) form and APAIS (Amsterdam Preoperative Anxiety and İnformation Scale) scale were filled in for all preoperative patients. Afterwards, the patients were treated with either midazolam or dexmedetothymidine, depending on the anesthesiologist's preference. After administration, he was taken to surgery. As intraoperative analgesics, 2 mg/kg tramadol and 15 mg/kg paracetamol were administered to all patients. postoperative recovery time (aldrete 10), 1., 2.,6.,12.,24. VAS score, postoperative nausea-vomiting scale, STAI-1(State Trait Anxiety İnventory ) form, first need time if postoperative analgesic was needed, and 24-hour total analgesic consumption were recorded. It was aimed to examine the effects of different premedications on postoperative pain and anxiety
Investigators
Seyda ARI
Doctor
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Eligibility Criteria
Inclusion Criteria
- •ASA 1-2-3
- •18-65 aged
- •Female patients
Exclusion Criteria
- •Under 18 years old and over 65 years old
- •Having a history of cerebrovascular disease illiteracy
- •Have visual and auditory problems İnability to cooperate with cognitive function test
- •Having emergency surgery
- •Those who are unable to read, understand and sign the consent form
- •Patients deemed unsuitable by the investigator
Arms & Interventions
low dose midazolam
0,025 mg/kg Midazolam
Intervention: Precedex and dormicum
high dose midazolam
0,05 mg/kg Midazolam
Intervention: Precedex and dormicum
low dose dexmedetothymidine
0.5 mg/kg dexmedetothymidine 10 minute infusion
Intervention: Precedex and dormicum
high dose dexmedetothymidine
1mg/kg dexmedetothymidine 10 minute infusion
Intervention: Precedex and dormicum
Outcomes
Primary Outcomes
effect of premedication on postoperative pain and anxiety scores
Time Frame: November 2022-December 2022