MedPath

Intrathecal Dexmedetomidine vs Epinephrine

Phase 4
Recruiting
Conditions
Cesarean Section
Anesthesia, Spinal
Interventions
Drug: Standardized Spinal Mixture
Registration Number
NCT06418308
Lead Sponsor
Icahn School of Medicine at Mount Sinai
Brief Summary

Several studies have shown that adding dexmedetomidine or epinephrine to single-dose spinal analgesia preparations improves the length and/or speed of onset of the sensory block and post-operative pain management without increased negative side effects. To date, however, no study has compared adjunctive intrathecal dexmedetomidine to adjunctive intrathecal epinephrine in single-dose spinal analgesia. The purpose of this study is to determine if adjunctive intrathecal dexmedetomidine is non-inferior to adjunctive intrathecal epinephrine in providing better single-dose spinal analgesia during cesarean section.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
90
Inclusion Criteria
  • Pregnant patients aged 18-55 years who are presenting for scheduled cesarean section and are candidates for single shot spinal anesthesia for cesarean section.
Exclusion Criteria
  • Patient refusal of spinal anesthetic
  • If patient is not a candidate for spinal anesthesia due to history of coagulopathy, elevated intracranial pressure, infection at site of injection, etc.
  • Emergency cesarean section
  • Preexisting motor or sensory deficit
  • Suspected pre-eclampsia
  • Patient receiving combined spinal-epidural as anesthetic technique

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DexmedetomidineDexmedetomidinereceiving the addition of 5 mcg of dexmedetomidine to the standard spinal medication mixture.
DexmedetomidineStandardized Spinal Mixturereceiving the addition of 5 mcg of dexmedetomidine to the standard spinal medication mixture.
EpinephrineEpinephrinereceiving the addition of 200 mcg of epinephrine to the standard spinal medication mixture
EpinephrineStandardized Spinal Mixturereceiving the addition of 200 mcg of epinephrine to the standard spinal medication mixture
Primary Outcome Measures
NameTimeMethod
Time required for sensory recovery270 minutes

Investigate the efficacy of intrathecal epinephrine versus dexmedetomidine as adjuvant agents in cesarean section. Once the sensory block to pinprick has receded to a T10 level, the spinal is no longer as effective for surgical level pain relief. This is a measure of the duration of the spinal as an effective analgesic. Sensory recovery will be a T10 level. This will be measured in minutes.

Secondary Outcome Measures
NameTimeMethod
Time to Bromage Score 1270 minutes

Time to motor recovery determines how long the patient will be in the post anesthesia care unit. This will be measured in minutes. Bromage Scale to determine recovery where recovery will be Bromage 1.

Bromage Scale:

Bromage 0 full flexion knees and feet

Bromage 1 just able to move knees

Bromage 2 able to move feet only

Bromage 3 unable to move feet or knees

Blood Pressure30 minutes

Systolic and Diastolic Blood pressures will be measured preoperatively and then every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement.

Phenylephrine Infusion Rate2 to 30 minutes

the phenylephrine infusion rate from 2 to 30 minutes after spinal placement

Total Phenylephrine Infusionduring surgery which can go up to 150 minutes

the total phenylephrine infusion given during surgery.

Number of Phenylephrine Bolusesduring surgery which can go up to 150 minutes

Number of Phenylephrine Boluses given during the operation

Number of Ephedrine Bolusesduring surgery which can go up to 150 minutes

Number of Ephedrine Boluses given during the operation

Number of Nausea episodes60 minutes

Nausea will be assessed every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement. If patient self-reports or exhibits any of these symptoms after 30 minutes while still in OR, this will also be recorded until patient is in PACU.

Number of Vomiting episodes60 minutes

Vomiting will be assessed every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement. If patient self-reports or exhibits any of these symptoms after 30 minutes while still in OR, this will also be recorded until patient is in PACU.

Number of Shivering episodes60 minutes

Shivering will be assessed every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement. If patient self-reports or exhibits any of these symptoms after 30 minutes while still in OR, this will also be recorded until patient is in PACU.

Number of Pruritus episodes60 minutes

Pruritus will be assessed every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement. If patient self-reports or exhibits any of these symptoms after 30 minutes while still in OR, this will also be recorded until patient is in PACU.

Pain Score at Skin Incisionwithin the surgery, which can go up to 150 minutes

Pain scores at time of skin incision. Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Pain Score at Uterine Incisionwithin the surgery, which can go up to 150 minutes

Pain scores at time of uterine incision. Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Pain Score at Uterine Exteriorizationwithin the surgery, which can go up to 150 minutes

Pain scores at time of uterine exteriorization. Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Pain Score at Uterine Closurewithin the surgery, which can go up to 150 minutes

Pain scores at time of uterine closure. Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Pain Score at Gutter Cleaningwithin the surgery, which can go up to 150 minutes

Pain scores at time of gutter cleaning. Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Pain Score at Procedure Finishat procedure finish, which can go up to 150 minutes

Pain scores at time of procedure finish . Pain will be graded on a scale of 0-10 (0 being no pain and 10 being the worst pain imaginable).

Additional IV Medicationduring surgery which can go up to 150 minutes

Any additional IV medications that need to be given during the surgery will be recorded (e.g. IV fentanyl).

Number of participants who require Conversion to General Anesthesiaduring surgery which can go up to 150 minutes

Number of participants who require Conversion to General Anesthesia. If converted to general anesthesia, enrollment in study will end.

Heart Ratetotal of 30 minutes from the time of spinal placement.

Heart rate will be measured every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement.

Oxygen Saturationtotal of 30 minutes from the time of spinal placement.

Oxygen saturation will be measured every 2 minutes for 10 minutes then every 5 minutes for a total of 30 minutes from the time of spinal placement.

Apgar Scores1 minute and 5 minutes

Neonatal Apgar Scores at 1 and 5 minutes will be recorded. Apgar score ranges from 0 to 10, with higher score indicating better health outcomes.

Number of NICU admissionDay 1

Number of babies that require Neonatal Intensive Care Unit (NICU) admission from the OR.

Patient Satisfaction ScorePost-Op Day 1

Patient will be asked to score satisfaction postoperatively Patient Satisfaction Score

1. Completely dissatisfied

2. Partially dissatisfied

3. Neutral

4. Partially satisfied

5. Completely satisfied

Time to First opioid24 hours

Via chart review, time to first opioid within a 24 hour time period after spinal placement.

Total Opioid Dose24 hours

Via chart review, time to total opioids given within a 24 hour time period after spinal placement.

Time to sensory block20 minutes

Spinal Onset - The T4 sensory level is considered adequate for operative analgesia for cesarean delivery. Time to a sensory block to pinprick to T4 level over a 20 minute time period after spinal placement will be recorded. If T4 not reached, highest level achieved will be recorded. This will be measured in minutes.

Trial Locations

Locations (1)

Mount Sinai Hospital

🇺🇸

New York, New York, United States

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