Comparing scalp block and incisional infiltration for pain management after craniotomy
Comparison Of The Effect Of Scalp Block And Incision Sıte Infiltratıon Applied On Postoperative Acute Paın And Hemodynamics In Patients Undergoing Craniotomy
NA · Aydin Adnan Menderes University · NCT06264765
This study is testing whether a scalp block or an injection at the incision site works better for managing pain after brain surgery in adults.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 62 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Aydin Adnan Menderes University (other) |
| Locations | 1 site (Aydın) |
| Trial ID | NCT06264765 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of scalp block versus incisional infiltration for managing postoperative pain in patients undergoing craniotomy. The study will involve routine anesthesia induction followed by either a scalp block or incisional infiltration before surgery begins. The primary focus is on assessing postoperative pain levels and hemodynamic stability, as both techniques have shown potential benefits in previous studies. The trial will include patients aged 18-75 with a Glasgow Coma Scale score greater than 13 who are undergoing elective craniotomy.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 18-75 who are undergoing elective craniotomy and have a Glasgow Coma Scale score greater than 13.
Not a fit: Patients who may not benefit from this study include those with a Glasgow Coma Scale score less than 13, emergency surgery cases, or those with contraindications to local anesthetics.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and reduced opioid consumption for patients after craniotomy.
How similar studies have performed: While there are limited studies directly comparing scalp block with incisional infiltration, existing research suggests both techniques can provide effective pain management and hemodynamic stability.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients who underwent craniotomy under elective conditions 2. ASA I-III 3. 18-75 years old 4. GCS \>13 Exclusion Criteria: 1. GCS \<13 2. Emergency surgery 3. Presence of contraindications to the LA agents used in this study 4. Chronic use of opioids 5. Psychiatric disorders 6. Presence of infection at the injection site 7. Uncontrolled intracranial hypertension 8. Chronic hypertension, 9. Coronary artery disease, arrhythmia, 10. Coagulopathy, 11. Patients who have previously undergone craniotomy
Where this trial is running
Aydın
- Ferdi Gülaştı — Aydın, Turkey (RECRUITING)
Study contacts
- Principal investigator: ferdi gülasştı — Aydin Adnan Menderes University
- Study coordinator: ferdi gülaştı
- Email: ferdigulasti@gmail.com
- Phone: 5054929650
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Hemodynamic Instability, scalp block, opioid consumption, postoperative pain