Analgesia, Obstetrical Clinical Trial
Official title:
Intrathecal Morphine Versus Intrathecal Hydromorphone for Analgesia Following Cesarean Delivery
Intrathecal (IT) opioids are commonly administered with local anesthetic during spinal anesthesia for post-Cesarean delivery analgesia. Traditionally, IT morphine has been used but the use of IT hydromorphone is growing. A previous study has shown that the effective dose for postoperative analgesia in 90% patients (ED90) for both IT hydromorphone and IT morphine (NCT02009722). These doses were found to be 75 mcg for hydromorphone and 150 mcg for morphine. The current proposed study would compare the duration of analgesia of IT morphine vs IT hydromorphone after elective cesarean delivery. Additionally, the investigators will compare each drug with respect the incidence of nausea and pruritus.
Spinal anesthesia is the most common anesthetic technique used for Cesarean delivery in the
United States and across the world. Intrathecal opioids are administered with a local
anesthetic during spinal anesthesia post-Cesarean delivery analgesia. The effectiveness of
intrathecal morphine for post-Cesarean pain control is well established, and the use of
intrathecal hydromorphone in this patient population is growing. No prospective studies have
been conducted to specifically compare the efficacy of intrathecal morphine versus
hydromorphone for post-Cesarean analgesia.
After intrathecal administration, opioid drug disposition depends on the lipid solubility of
the individual drug. Because of its hydrophilic nature, cerebrospinal fluid (CSF)
concentrations of morphine decline more slowly than similar doses of lipophilic drugs. This
accounts for more rostral spread, greater dermatomal analgesia, and longer duration of action
when compared to highly lipophilic opioids like fentanyl and sufentanil. When used for
post-cesarean analgesia, intrathecal morphine has a duration of action between 14-36 hours
with wide variation between individual patients. While hydromorphone is similar chemically to
morphine, it is more lipid soluble. This decreases its spread within the intrathecal space
and enhances its penetration into the dorsal horn of the spinal cord where interactions with
opioid receptors occur. These differences between the two medications may influence their
duration of action. Theoretically, this would reduce the duration of action of intrathecal
hydromorphone when compared with intrathecal morphine. Retrospective studies have shown that
the analgesic benefit for intrathecal hydromorphone appears to extend at least 12 hours after
cesarean delivery and may extend up to 24 hours.
Although effective in reducing pain, intrathecal opioids are associated with side effects
including pruritus, nausea, and respiratory depression. A meta-analysis reviewing
twenty-eight studies which investigated intrathecal morphine versus placebo demonstrated
moderate increases in the incidences of pruritus, nausea and vomiting. In fact the incidence
of nausea with IT morphine has been reported to be nearly 33%. The differences in
pharmacokinetics between morphine and hydromorphone may also create differences in side
effect profiles. Some studies have found that hydromorphone causes less nausea and pruritus
than morphine, while others have not. Although opioid-induced respiratory depression is a
rare event, studies evaluating intrathecal hydromorphone for post-Cesarean delivery pain have
not reported any cases of respiratory depression.
In this study, the investigators aim to compare the duration of analgesia of intrathecal
morphine vs. hydromorphone for analgesia after cesarean delivery. Secondarily, the
investigators will compare the side effects of each drug, including nausea and pruritus. To
achieve the goals of this study, it is important to study equipotent doses of these
medications. Previous work by the investigators of this study found that the effective dose
for postoperative analgesia in 90% of patients (ED90) is 75 micrograms for intrathecal
hydromorphone and 150 micrograms for intrathecal morphine. However, it is not known if these
two equipotent medication doses provide a similar duration of analgesia.
The investigators hypothesize that 150 mcg of intrathecal morphine will result in a longer
duration of analgesia when compared to 75 micrograms of intrathecal hydromorphone.
Additionally, the investigators hypothesize that there will be more pruritus in the
intrathecal hydromorphone group early after surgery, and no difference in side effects at 24
hours after surgery.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT02557087 -
Hyoscine ButylBromide for Intrapartum Analgesia
|
Phase 2 | |
Not yet recruiting |
NCT02578251 -
Paracetamol for Intrapartum Analgesia
|
Phase 2 | |
Recruiting |
NCT06236126 -
SKIN WHEAL - Subcutaneous or Intradermal Lidocaine in Epidural for Laboring Pain.
|
N/A | |
Completed |
NCT02509312 -
Prospective Effect of Intravenous Ketorolac on Opioid Use, EBL and Complications Following Cesarean Delivery
|
Phase 4 | |
Completed |
NCT05099055 -
Dexmedetomine as Adjuvant for Spinal Anesthesia in Elective Cesarian Sections : a Pilot Study
|
Phase 3 | |
Active, not recruiting |
NCT03167905 -
CODEPAD (Collaborative Outcomes of DEpression and Pain Associated With Delivery)
|
Phase 2/Phase 3 | |
Completed |
NCT02009722 -
Intrathecal Opioids for Pain Control After Cesarean Delivery: Determining the Optimal Dose
|
Phase 4 | |
Active, not recruiting |
NCT03805607 -
IV Ketorolac on Platelet Function Post-Cesarean Delivery
|
Phase 4 | |
Completed |
NCT03574441 -
Intrapartum Epidural Catheter Displacement: Dressing Methods
|
N/A | |
Completed |
NCT02920489 -
Individualized Timing of Analgesia and Effectiveness of Labor Analgesia
|
N/A | |
Completed |
NCT02823418 -
Neuraxial Labor Analgesia and the Incidence of Postpartum Depression
|
||
Not yet recruiting |
NCT05977361 -
Intrathecal Catheter Placement Versus Resiting Epidural Catheter After Dural Puncture in Obstetric Patients
|
N/A |