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Search / Trial NCT06883279

Effect of Interscalene Block Methods on Rebound Pain

Launched by ANKARA CITY HOSPITAL BILKENT · Mar 12, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Anesthesia Interscalene Block Rebound Pain

ClinConnect Summary

This clinical trial is studying how different methods of providing anesthesia might affect a type of pain called "rebound pain" after shoulder surgery. Rebound pain is a sudden and intense pain that some patients experience right after the anesthesia wears off. The researchers want to see if using a specific technique to deliver local anesthesia—one that doesn’t directly inject into the nerve root—can help reduce this rebound pain in patients undergoing arthroscopic shoulder surgery.

To participate in this trial, you must be between 18 and 65 years old and be in good health (ASA physical status I or II). If you are planning to have shoulder surgery in a certain position and need an interscalene nerve block for anesthesia, you might be eligible. Participants will receive the anesthesia and will be monitored for any rebound pain using a simple pain scale. It’s important to note that there are some exclusions, such as certain health conditions and previous surgeries on the shoulder, so not everyone will qualify. If you join the study, you can help improve pain management for future patients undergoing similar procedures.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients aged 18-65 years.
  • Patients with ASA physical status I or II.
  • Patients planned for arthroscopic shoulder surgery in the lateral decubitus position with interscalene nerve block.
  • Exclusion Criteria:
  • Patients who do not consent to participate in the study.
  • Block failure.
  • Language acquisition deficiency.
  • Obesity (body mass index \> 35 kg/m²).
  • Diabetes.
  • Psychiatric disorders.
  • Central nervous system diseases.
  • Vestibular diseases.
  • Presence of neuropathy and paralysis.
  • Pregnancy.
  • Previous open shoulder surgery.
  • Allergy to local anesthetics.
  • Coagulopathy.
  • Severe thrombocytopenia.
  • Infection at the puncture site.
  • Pre-existing neuropathy in the limb to be operated.
  • Use of dexamethasone.
  • Use of opioid and antiemetic medications before surgery.
  • Severe cardiopulmonary disease.
  • Low baseline oxygen saturation.
  • Conditions that prevent cooperation in the postoperative period (e.g., mental retardation, delirium).

About Ankara City Hospital Bilkent

Ankara City Hospital Bilkent is a leading healthcare institution in Turkey, dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. Equipped with state-of-the-art facilities and a multidisciplinary team of experienced professionals, the hospital fosters a collaborative environment for conducting rigorous scientific investigations. Its commitment to ethical standards and patient safety ensures that all clinical trials are conducted with the highest level of integrity, ultimately contributing to the development of new therapies and enhancing the quality of care provided to patients.

Locations

Ankara, , Turkey

Ankara, Ankara, çankaya, Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported