REDUCE Trial: Perineural Dexamethasone on Scalp Nerve Blocks
- Conditions
- Postoperative PainCraniotomyDexamethasoneScalp Nerve Blocks
- Interventions
- Registration Number
- NCT04648358
- Lead Sponsor
- Beijing Tiantan Hospital
- Brief Summary
Pain is common in the first 2 days after major craniotomy. Inadequate analgesia may lead to an increased risk of postoperative complications. Most pain following craniotomy arises from the pericranial muscles and soft tissues of the scalp. Scalp nerve blocks with local anesthesia seem to provide effective, safe, however transient postoperative analgesia which does not seem to meet the requirements of craniotomy. Currently, peripheral dexamethasone has been observed to significantly prolong the duration of analgesia of nerve blocks (e.g., saphenous nerve block, adductor canal block, thoracic paravertebral block, brachial plexus nerve block). On the contrary, a study reported that perineural dexamethasone did not appear to prolong the analgesic time after supratentorial craniotomy. However, all patients in this study were given 24 mg of oral or intravenous dexamethasone regularly at least 7 days during the perioperative period, which possibly masked the role of single local low doses of perineural dexamethasone. Therefore, the analgesic effect of single dexamethasone for scalp nerve blocks without the backdrop of perioperative glucocorticoid deserves further clarification.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 156
- scheduled for elective supratentorial craniotomy under general anesthesia;
- age 18 to 64 years;
- an American Society of Anesthesiologists (ASA) physical status of I, II or III;
- preoperative Glasgow Coma Scale (GCS) score of 15/15.
- History of chronic headache or chronic pain syndrome of any cause, psychiatric disorders, or uncontrolled epilepsy;
- Inability to understand or use the pain scales before surgery;
- Excessive alcohol or drug abuse, chronic opioid use (more than 2 weeks or 3 days per week for more than 1 month), use of drugs with confirmed or suspected sedative or analgesic effects, or use of any painkiller within 24 hours before surgery;
- Request of oral/intravenous glucocorticoid to decrease cerebral edema within 1 week before surgery;
- Pregnancy or breastfeeding;
- Extreme body mass index (BMI) (< 15 or > 35);
- Participation in another interventional trial that interferes with the intervention or outcome of this trial;
- Refusal or inability of the patient and/or legal guardian to provide informed consent;
- Coagulopathy;
- Infection around the puncture point;
- History of allergies to any of the study drugs.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description DEX4mg group Dexamethasone combined with bupivacaine DEX4mg group will receive scalp nerve blocks with 0.5% bupivacaine, plus 4 mg dexamethasone with epinephrine at 1:200,000. Control group Bupivacaine The control group will receive scalp nerve blocks with 0.5% bupivacaine, plus normal saline with epinephrine at 1:200,000
- Primary Outcome Measures
Name Time Method The duration of analgesia Within 48 hours after surgery The time between the performance of the block and the administration of the first press the PCA demand button postoperatively.
- Secondary Outcome Measures
Name Time Method Bradycardia Within 48 hours after surgery Bradycardia will be defined as HR\<60 beats/minute in at least two instances more than 5 minutes apart.
Postoperative nausea and vomiting (PONV) Within 48 hours after surgery Vomiting will be defined as the forceful expulsion of gastric contents, and nausea will be defined as an unpleasant sensation associated with the urge to vomit.
Patient satisfaction score (PSS) At 2, 4, 8, 12, 16, 20, 24, and 48 hours postoperatively PSS: 0 for unsatisfactory to 10 for very satisfactory.
Sufentanil consumption At 4, 12, 24 and 48 hours postoperatively The cumulative amount of sufentanil consumption by PCA
Glasgow Coma Scale (GCS) At 2, 4, 8, 12, 16, 20, 24, and 48 hours postoperatively A scale for measuring level of consciousness, in which scoring is determined by three factors: amount of eye opening, verbal responsiveness, and motor responsiveness.
Numeric rating scale (NRS) At 2, 4, 8, 12, 16, 20, 24, and 48 hours postoperatively NRS: 11-point scale in which 0 = no pain to 10 = worst imaginable pain. An NRS score ≥4 will be considered significant or moderate pain. An NRS score ≥7 will be considered severe pain. Meanwhile, the localization of the site of the pain will also be documented.
Hypotension Within 48 hours after surgery Hypotension will be defined as any of the following: systolic BP \<90 mm Hg for 5 minutes or a 35% decrease in mean arterial blood pressure.
The length of stay (LOS) About at 2 weeks after surgery The LOS will be defined as the number of nights spent in the hospital after surgery.
Emergence delirium Within 48 hours after surgery Emergence delirium will be assessed by the Sedation Agitation Scale (SAS), a 7-point scale on which a higher score represents greater agitation.
Trial Locations
- Locations (1)
Beijing Tiantan Hospital
🇨🇳Beijing, Beijing, China