SummaryThis randomised controlled trial examines the effects of fentanyl and diamorphine, alone and in combination, as adjuncts to spinal anaesthesia for Caesarean section. Ninety-nine women undergoing elective Caesarean section with spinal anaesthesia using 0.5% hyperbaric bupivacaine were randomly allocated to receive fentanyl 15 lg (F), diamorphine 0.25 mg (D), or fentanyl 15 lg plus diamorphine 0.25 mg (FD), intrathecally. All women received morphine via a patient controlled analgesia system after surgery. There was no significant difference between the groups in time to achieve a block, discomfort, ephedrine use, nausea and vomiting, pruritus and sedation during surgery. Significant differences were observed in morphine consumption 4, 8, 12 and 24 h after surgery between both F and D groups, and F and FD groups, and also at 2 h between F and FD groups. There was a significant difference in pruritus at 4 h between the F and FD group. Our results suggest that diamorphine alone provides optimum benefits during and after surgery, when used in combination with hyperbaric bupivacaine for Caesarean section. Since the discovery of opiate receptors in the brain and spinal cord, the use of intrathecal opioids has become common practice as an effective method of analgesia. No area has utilised this knowledge more than obstetric anaesthesia and the benefits of intrathecal opioids as adjuncts in anaesthesia for Caesarean section (LSCS) are well documented.The use of intrathecal fentanyl as an adjunct during surgery in LSCS has many advantages, namely, improving the quality of spinal anaesthesia [1][2][3] and decreasing the time to establish the block [1]. The use of fentanyl has also been shown to have a bupivacaine-sparing effect [4,5] and therefore leads to fewer episodes of hypotension during surgery.In contrast, the lipophobic opiate morphine has many beneficial effects of its own. Many studies have shown that intrathecal morphine can produce excellent analgesia after surgery [6,7], and it is therefore often used in combination with fentanyl.