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Published on: July 16, 2014
Clonidine addition prolongs the duration of caudal analgesia
T S Yildiz1, F Korkmaz, M Solak
1Department of Anaesthesiology, School of Medicine, University of Kocaeli, Kocaeli, Turkey. tulaysahin00@yahoo.com
Insights
Adding clonidine to bupivacaine in caudal anesthesia significantly extends post-operative pain relief in children. This combination provides prolonged analgesia without adverse respiratory or hemodynamic effects.
Area of Science:
- Pediatric Anesthesiology
- Pharmacology
Background:
- Post-operative pain management in children is crucial for recovery.
- Caudal anesthesia with bupivacaine is a common method for pediatric surgical procedures.
- Optimizing the duration of analgesia is a key clinical goal.
Purpose of the Study:
- To evaluate the efficacy of clonidine as an adjunct to bupivacaine in caudal anesthesia.
- To determine the optimal dose of clonidine for prolonging post-operative analgesia in children.
- To assess the safety profile of clonidine when combined with bupivacaine.
Main Methods:
- A prospective, double-blind, randomized controlled trial involving 60 children (1-10 years) undergoing inguinal hernia repair.
- Children received caudal anesthesia with 0.125% bupivacaine plus varying doses of clonidine (0, 1, 1.5, or 2 microg/kg).
- Pain was assessed using the modified Children's Hospital of Eastern Ontario Pain Scale (mCHEOPS) and visual analogue scale (VAS); hemodynamic parameters and respiratory function were monitored.
Main Results:
- The group receiving 2 microg/kg of clonidine demonstrated a significantly longer duration of analgesia (median 650 min).
- No instances of peri-operative hypotension, bradycardia, post-operative respiratory depression, or motor block were observed.
- The addition of clonidine did not increase adverse events.
Conclusions:
- Clonidine is a safe and effective adjunct to bupivacaine in caudal anesthesia for pediatric patients.
- The 2 microg/kg dose of clonidine significantly prolongs post-operative analgesia duration.
- This combination offers an improved pain management strategy with no compromise on patient safety.
Background:
In this study, using a dose-ranging design, we examined the effects of clonidine with 0.125% bupivacaine on the duration of post-operative analgesia in caudal anaesthesia in children.
Methods:
We conducted a controlled, prospective study of clonidine in caudal anaesthesia in 60 children, aged 1-10 years, undergoing elective inguinal hernia repair. Induction and maintenance of anaesthesia were performed by inhalation of sevoflurane and nitrous oxide. The children were randomized in a double-blind fashion to four groups, and were given a caudal anaesthetic with either 0.125% plain isobaric bupivacaine (1 ml/kg) or bupivacaine plus 1, 1.5 or 2 microg/kg of clonidine. The blood pressure and heart rate were recorded peri-operatively. Analgesia was evaluated by the modified Children's Hospital of Eastern Ontario Pain Scale (mCHEOPS) or a visual analogue scale (VAS). Paracetamol was given when the mCHEOPS score was greater than five or when the VAS score was greater than 30 mm. The monitoring of scores for pain, haemodynamic changes and post-operative nausea and vomiting was performed by nurses blind to the study allocation.
Results:
The duration of analgesia was found to be significantly longer in the group given bupivacaine plus 2 microg/kg of clonidine (median, 650 min; range, 300-900 min). Peri-operative hypotension and bradycardia, post-operative respiratory depression and motor block were not recorded in any patient.
Conclusions:
The addition of clonidine to 0.125% bupivacaine prolongs the duration of post-operative analgesia without any respiratory or haemodynamic side-effects.
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