Evaluation of Postoperative Pain Control in Ear Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKocaeli University
About this trial
Middle ear surgery is the most popular procedure in ear, nose and throat surgery. Increased sympathetic stimulation after surgery can activate the sympathetic system, causing hypertension and increased heart rate. As a result of these clinical conditions, hemorrhage can occur, which can impair the quality of the surgical field, which is undesirable in middle ear surgery.Clinical studies should be conducted with auricularis magnus nerve block applied in the perioperative period in middle ear surgery and postoperative pain scores.
Eligibility criteria
Qualifiers
Patients undergoing CWD and Mastodectom
Patients undergoing elective surgery
ASA (American Society of Anesthesiologists) physical status classification I-II
Patients over 18 years of age
Disqualifiers
Anticoagulant use
Allergy to the drugs to be used
ASA (American Society of Anesthesiologists) physical status classification IV-V
Presence of infection in the area where the block will be applied
Trial design
Treatments tested in this trial
- Auricularis Magnus Nerve Block
- Control Group
Treatment groups
56 Participants
are divided into 2 treatment groupsSponsors and collaborators
Kocaeli University
Lead sponsor
Başakşehir Çam & Sakura City Hospital
Sponsor institution
Başakşehir Çam & Sakura City Hospital
Collaborator
Source ClinicalTrials.gov