Multimodal Pain Management for Cesarean Delivery

Pain Clinical Trial

Official title:

Multimodal Pain Management for Cesarean Delivery: A Randomized Control Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02922985
• Other study ID #: IRB 16-0121
• Status: Completed
• Phase: Phase 4
• Start date: October 2016
• Est. completion date: July 2017

Study information

• Verified date: October 2017
• Source: The University of Texas Medical Branch, Galveston
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Opioid use and abuse has become a major medical problem in the United States. Over prescription of opioid medications is a major contributor to this growing problem. Cesarean delivery (CD) is the most commonly performed surgery in the US and women are generally given opioid medications for postoperative pain management. This is not a common practice in other developed countries. We believe that a multimodal pain management strategy is superior to current practices for control of postoperative pain after CD and will lead to a decrease in the use of opioid medications. This will have beneficial effects on patients' recovery and bonding with their newborns, as well as societal effects in reducing the burden of opioid abuse in the US. Our objective is to investigate the use of a multimodal pain regimen in pregnant patients undergoing CD. This is a randomized double-blinded, placebo controlled trial. The multimodal intervention consists of a pre-operative dose of IV acetaminophen (Ofirmev), infiltration of subcutaneous bupivacaine prior to skin incision, and a dose of IM ketorolac at time of fascial closure. These study medications are currently used in our patient population but not in a standardized fashion, not in every patient, and not always in combination with each other. The control group will receive placebo IV infusion preoperatively and an IM injection at fascial closure, and subcutaneous infiltration with normal saline before skin incision. Both groups will receive spinal regional anesthesia as per anesthesia team and then postoperatively, both groups will receive the current standard of care, which consists postoperative hydrocodone/acetaminophen and ibuprofen as needed depending on pain score. Our primary outcome of interest will be the total opioid intake in the first 48 hours after surgery. Secondary outcomes include time to first opioid given, pain scores at 6-12, 24 and 48 hours post op, and total number of opioid tablets left after discharge on post op day number 7. We will also evaluate patient satisfaction scores and total length of hospital stay. We will evaluate neonatal outcomes including Apgar scores, cord blood gases, immediate newborn complications in the first 48 hours after birth, and any infant adverse outcomes related to maternal opioid use up to 4 weeks of life. Our hypothesis is that our multimodal pain regimen will decrease the total opioid requirement in the first 48 hours after surgery.

Description:

We are proposing a double-blinded, placebo controlled, randomized trial of patients undergoing elective cesarean delivery. Participants will be randomized to either a control group or study group. This is a double-blinded study, neither participants nor the obstetric or anesthesia team are aware of study assignment. The study group, aka multimodal group, will receive 1 g of IV acetaminophen (ofirmev) within 30 minutes before starting the surgery, regional anesthesia (spinal anesthesia only) with fentanyl, duramorph (morphine) and bupivacaine will be performed as per anesthesia team, the anticipated sight of skin incision will be infiltrated with 20 mL of bupivacaine 0.25% in the subcutaneous space prior to skin incision, and 60 mg of intramuscular (IM) ketorolac (toradol) will be given at the time of fascial closure. The control group will receive a placebo drip within 30 minutes before starting the surgery, regional anesthesia (spinal anesthesia only) with fentanyl, duramorph (morphine) and bupivacaine will be performed as per anesthesia team, the anticipated sight of skin incision will be infiltrated with 20 mL of normal saline in the subcutaneous space prior to skin incision, and an IM dose of placebo at the time of fascial closure. Post-operatively both groups will be managed similarly.

Inclusion Criteria:

• Women who are 18 - 45 years of age at the time of cesarean delivery with the ability to give informed consent

• Elective cesarean delivery

• Gestational age ≥ 34 weeks

• Fluent in either English or Spanish

• Spinal anesthesia

Exclusion Criteria:

Urgent or emergent CD Active labor Epidural or Intrathecal regional anesthesia General anesthesia Patients with a contraindication for regional anesthesia Acute or chronic hepatic disease Acute or chronic renal disease Active asthma Gastrointestinal ulceration Inflammatory bowel disease Allergy to ketorolac, acetaminophen, hydrocodone, codeine, ibuprofen or bupivacaine Opioid dependence Non reassuring fetal or maternal status requiring immediate delivery Placenta previa or accreta Acute or chronic pain disorder Maternal weight <50 kilograms Uncontrolled hypertension Ischemic cardiac disease Congestive heart failure Thrombocytopenia, platelet count <150,000/microliter Preeclampsia including Hemolysis Elevated Liver enzymes Low Platelets syndrome DIC or active hemorrhage before randomization Estimated blood loss > 2000 mL

Primary Outcome: The primary outcome of the study is the total opioid (hydrocodone) use in milligrams in the first 48 hours after cesarean delivery.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 120
• Est. completion date: July 2017
• Est. primary completion date: June 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Women who are 18 - 45 years of age at the time of cesarean delivery with the ability to give informed consent

• Elective cesarean delivery

• Gestational age = 34 weeks

• Fluent in either English or Spanish

• Spinal anesthesia

Exclusion Criteria:

• Urgent or emergent CD

• Epidural or combined spinal epidural regional anesthesia

• General anesthesia

• Patients with a contraindication for regional anesthesia

• Acute or chronic hepatic disease

• Acute or chronic renal disease

• Active asthma

• Gastrointestinal ulceration

• Inflammatory bowel disease

• Allergy to ketorolac, acetaminophen, hydrocodone, codeine, ibuprofen or bupivacaine

• Opioid dependence

• Non reassuring fetal or maternal status requiring immediate delivery

• Placenta previa or accreta

• Acute or chronic pain disorder

• Maternal weight <50 kilograms

• Uncontrolled hypertension

• Ischemic cardiac disease

• Congestive heart failure

• Thrombocytopenia, platelet count <150,000/microliter

• Preeclampsia including Hemolysis Elevated Liver enzymes Low Platelets syndrome

• Disseminated intravascular coagulation (DIC) or active hemorrhage before randomization

• Estimated blood loss > 2000 mL

Related Conditions & MeSH terms

• Pain

Intervention

Drug:
• Intravenous acetominophen
One dose if 1 gram intravenous to be given pre-surgery
• Ketorolac, intramuscular
One dose of 60 mg Intramuscular to be given at time of skin closure
• Bupivacaine, subcutaneous
Inject 20 mL of 0.25% bupivacaine at the site of anticipated skin incision.
• Normal saline
Normal saline will be given intravenously, intra-muscularly, and subcutaneously in the same volume as the study drugs for the patients in the placebo group.

Locations

Country	Name	City	State
United States	University of Texas Medical Branch	Galveston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
The University of Texas Medical Branch, Galveston

Country where clinical trial is conducted

United States, 

References & Publications (4)

Bartels K, Mayes LM, Dingmann C, Bullard KJ, Hopfer CJ, Binswanger IA. Opioid Use and Storage Patterns by Patients after Hospital Discharge following Surgery. PLoS One. 2016 Jan 29;11(1):e0147972. doi: 10.1371/journal.pone.0147972. eCollection 2016. — View Citation

Munishankar B, Fettes P, Moore C, McLeod GA. A double-blind randomised controlled trial of paracetamol, diclofenac or the combination for pain relief after caesarean section. Int J Obstet Anesth. 2008 Jan;17(1):9-14. Epub 2007 Nov 5. — View Citation

Rosaeg OP, Lui AC, Cicutti NJ, Bragg PR, Crossan ML, Krepski B. Peri-operative multimodal pain therapy for caesarean section: analgesia and fitness for discharge. Can J Anaesth. 1997 Aug;44(8):803-9. — View Citation

Santoso JT, Ulm MA, Jennings PW, Wan JY. Multimodal pain control is associated with reduced hospital stay following open abdominal hysterectomy. Eur J Obstet Gynecol Reprod Biol. 2014 Dec;183:48-51. doi: 10.1016/j.ejogrb.2014.10.007. Epub 2014 Oct 14. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Total Opioid Intake in Morphine Milligram Equivalents in the First 48 Hours After Cesarean Delivery (CD)	Every opioid intake by the patient in the first 48 hours after CD will be recorded and quantified in morphine milligram equivalents	48 hours post cesarean delivery
Secondary	Time to First Administration of Opioid Pain Medication Post Operatively	Time, in hours, to first administration of opioid pain medication post operatively	48 hours post cesarean delivery
Secondary	Pain Score at 6-12 Hours Post Operatively	Pain score at 6-12 hours post-operatively, expressed on a pain scale from 0-10 with the higher score meaning worse pain (outcome).	6-12 hours post-operatively
Secondary	Number of Opioid Pain Tablets Remaining on Post-operative Day #7 From the Discharge Prescription.	Number of opioid pain tablets remaining on post-operative day #7 from hospital discharge as reported by patients	7 days post delivery
Secondary	Hospital Length of Stay	Time to discharge from hospital, measured in hours	From time of hospital admission to time of discharge home up to 168 hours.
Secondary	Pain Score at 24 Hours Post-operatively	Pain Score at 24 Hours Post Operatively, expressed on a pain scale from 0-10 with the higher score meaning worse pain (outcome).	24 hours post-operatively
Secondary	Pain Score at 48 Hours Post-operatively	Pain Score at 48 Hours Post-operatively, expressed on a pain scale from 0-10 with the higher score meaning worse pain (outcome).	48 hours post-operatively
Secondary	Apgar Score at 5 Minutes	This is the Apgar score of the newborn collected at 5 minutes. Range is from 0-10, with the higher scores meaning a better outcome.	5 minutes after birth
Secondary	NICU Admission	Rate of admission to the neonatal intensive care unit	after birth and before hospital discharge
Secondary	Need for Respiratory Support	neonate receipt of oxygen by nasal cannula or mechanical ventilation	after birth and before hospital discharge