Health TrialsbyHealthPanel

Evaluation of Postoperative Pain Control in Ear Surgery

ConditionsPost Operative PainAnalgesia
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

This trial does not accept healthy volunteers

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

Design model

Crossover

Treatments tested in this trial

  • Auricularis Magnus Nerve Block

    Procedure/Surgery

    Auricularis Magnus Nerve block will be performed using 5 mL of %0.5 bupivacaine

  • Control Group

    Procedure/Surgery

    Intravenous analgesics 1 gram paracetamol, 20 mg tenoxicam, 8 mg ondansetron will be administered.

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: Auricularis Magnus Nerve BlockActive comparator 1 intervention
Group B: ControlActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Opioid consumption

Intraoperative opioid consumption

Time frame
During the operation

Secondary outcomes

1

Morphine consumption

Postoperative morphine consumption

Time frame
1 hours after surgery(T1), 6 hours after surgery (T2), 12 hours after surgery (T3), 24 hours after surgery (T4)
2

NRS Scores

NRS scores of the patients after the surgery (0=no pain, 10=worst pain imaginable)

Time frame
1 hours after surgery(T1), 6 hours after surgery (T2), 12 hours after surgery (T3), 24 hours after surgery (T4)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Kocaeli University

Lead sponsor

Başakşehir Çam & Sakura City Hospital

Sponsor institution

Başakşehir Çam & Sakura City Hospital

Collaborator

Source ClinicalTrials.gov
Apply now