CClinicalTrials.gg
CompletedNCT06091657Updated Jan 17, 2025

Comparison of Ketamine Plus Dexamethasone Versus Ketamine Alone for Prevention of Severe Shivering After Spinal Anesthesia in Cesarean Section

An interventional study of Ketamine Hydrochloride in Intraoperative Shivering, Ketamine With Shivering and Dexamethasone for Shivering, sponsored by Kasr El Aini Hospital. Completed at 1 site in Egypt. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2025-01-17.

Sponsored by Kasr El Aini Hospital · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

Shivering is one of the most distressing events of the birth experience for patients. Shivering that occurs with spinal anesthesia is a frequent event, with a reported incidence of up to 50-65%. (1) This may be normal thermoregulatory shivering in response to core hypothermia or may result from the release of cytokines by the surgical procedure. (2-4) shivering is graded with a scale described by Bedside Shivering Assessment Score (BSAS). (3, 4) Most of the literature recommends a variety of non-pharmacological and pharmacological options for the prevention and treatment of shivering after spinal anesthesia. Pethidine, tramadol, clonidine, dexmedetomidine, biogenic amines (serotonin 5-HT3 receptor antagonist), low-dose ketamine, dexamethasone, and magnesium sulfate were used as pharmacological agents. (5) Intravenous (IV) ketamine 0.25 mg/kg was approved as effective in the prevention and treatment of shivering after regional anesthesia and can be used in patients undergoing cesarean sections without adverse effects on the baby. (5) Ketamine is a competitive N-methyl-D-aspartate receptor antagonist, and it is believed that its anti-shivering action is due to non-shivering thermogenesis, either by effect on the hypothalamus or by the β-adrenergic effect of norepinephrine. (6) In spite of the approved effectiveness of ketamine in this issue, moderate to severe shivering (grade ≥ 2) still occurs with an incidence that cannot be ignored. (7-9) Dexamethasone was also approved as an alternative pharmacological agent for the prevention and treatment of mild and moderate shivering. (10) Dexamethasone prevents shivering by regulating immune response and decreasing the temperature gradient between skin and body core via its anti-inflammatory action and inhibition of the release of vasoconstrictors and pyrogenic cytokines. We hypothesize that addition of dexamethasone (0.1 mg\kg) to low dose ketamine (0.25 mg\kg) will be more effective in prevention of severe shivering after spinal anesthesia with cesarean section with minimal sedation of the mother and negligible effect on the baby. This can be applicable in resource-limited settings.

Read the detailed description
  • Preoperatively, a trained anesthetist will assess the patients regarding the age, height; weight. Medical history, medications, laboratory investigation, as well as the patient's airway. Fasting hours will be reviewed(8 hours) In the operating room; temperature will be maintained at 24 °c -26° c by adjusting the temperature setting of the air conditioner.
  • Routine monitors (electrocardiogram, pulse oximetry, and non-invasive blood pressure monitor) will be applied \& axillary temperature will be recorded; then intravenous access (18-G cannula) will be inserted and pre-medication ranitidine 40 mg will be administered.
  • Baseline vitalsigns will be recorded in the supine position. Ringer lactate infusion (which is kept at room temperature 24°c -26°c) will be started at a rate of 10 ml/kg for the first 30 minutes then reduced to 6 ml/kg till the end of the surgery.

B. drug preparation:

An independent research assistant will be responsible for opening the envelopes and preparing the study drug with no further involvement in the study. The attending anesthetist and data collector will be blinded to the study group.

Group K (ketamine):

syringe (1): the ketamine syringe, dilute 25 mg ketamine in 10 ml saline to have a concentration of 2.5mg/ml. The dose will be 0.25 mg/kg, so we will give 0.1ml/kg of the syringe.

syringe (2): saline syringe 10 ml saline in 10 ml syringe. (for double blinded technique). we will give 0.1ml/kg of the syringe.

Group KD (ketamine plus dexamethasone):

Syringes (1): the ketamine syringe, dilute 25 mg ketamine in 10 ml saline to have a concentration of 2.5mg/ml. The dose will be 0.25 mg/kg, so we will give 0.1ml/kg of the syringe.

Syringe (2): dexamethasone syringe, 10 mg dexamethasone will be diluted with 10 ml saline in 10 ml syringe, concentration will be 1mg/ml. the dose will be 0.1 mg/kg, so we will give 0.1ml/kg of the syringe.

The drugs will be given to the patient by direct intravenous injection through the cannula and flushing with normal saline after administration of the drugs.

Recording of vital signs (arterial blood pressure, heart rate, oxygen saturation axillary temperature) then shifting the patient to the sitting position with a nurse in front of her for administration of subarachnoid block In the sitting posture, a 25G Quincke's spinal needle is used to puncture the L3-L4 interspace under sterile conditions and via the midline route.

After the CSF free flow, 12-15 mg hyperbaric bupivacaine will be givenIntrathecal (according to the patient's height) and the patient will be placed in a supine posture with 15 degrees tilt to left side with a wedge under right iliac bone. Patients will be given 3 liters of oxygen per minute through the nasal cannula.

After spinal anesthesia , arterial blood pressure, heart rate and oxygen saturation will all be recorded immediately after shifting the patient to supine position.

Hypotension is defined as a drop in mean arterial blood pressure (more than 20% below baseline) following spinal injection, and it is treated by increasing intravenous fluid administration and administering 2.5-5 milligrams increments of ephedrine I.V. (every 3-5 minutes) until the hypotension is resolved.

After the sensory block at the level of T4-T6 is confirmed by the lack of sensitivity to cold, surgery will begin. The heart rate, oxygen saturation,are continuously monitored and the blood pressure readings will be taken every 10 minutes till the end of the surgery.

During surgery, a shivering score will be recorded at 15 min intervals and axillary temperature will be recorded after 30 minutes then at the end of the surgery.

Rescue dose of pethidine (25 mg) could be given intravenously if the participant developed grade 3 or grade 4 shivering

  • Apgar score of the baby will be recorded as a secondary outcome.
  • The level of sedation of the mother using The University of Michigan Sedation Scale (UMSS) will be recorded.

Post operative monitoring:

The participants will be monitored post-operatively for 60 minutes regarding their hemodynamics and shivering score.

Any complications in the Intra operative and post-operative period will be recorded.

  1. Measurement tools
  • Demographic data as age, sex, BMI, medications, drug allergy and any other comorbidity.
  • Heart rate, SpO2, and non-invasive arterial blood pressure will be monitored and recorded before spinal anesthesia and every 10 minutes after spinal anesthesia till the end of the procedure.
  • Length of operation and the number of shivering episodes scored ≥2 will be recorded.
  • Temperature: axillary temperature will be measured before, immediately and 30 minutes after induction of spinal anesthesia, and at the end of surgery.
  • Hemodynamics, temperature, shivering episodes will be recorded for 60 minutes postoperatively.
  • Bedside Shivering Assessment Scale shivering score will be recorded at 15 min intervals till the end of the procedure and for 60 minutes in post anesthesia care unit
  • Grade 0 if there is no shivering
  • Grade 1 if there is no muscle contraction but mild fasciculation of face or neck or peripheral vasoconstriction but no visible shivering
  • Grade 2 if there is a visible muscular activity in only one muscle group
  • Grade 3 if the muscular activity is in more than one muscle group but not generalized
  • Grade 4 if gross muscular activity involving the entire body.
  • The level of sedation of the mother will be recorded using The University of Michigan Sedation Scale (UMSS).

Table 1: The University of Michigan Sedation Scale (UMSS)(Liu et al., 2018) Value Patient state 0 • Awake and alert.

    • Minimally sedated: tired/ sleepy, appropriate response to verbal conversation, and/or sound.
    • Moderately sedated: somnolent/ sleeping, easily aroused with light tactile stimulation or a simple verbal command.
    • Deeply sedated: deep sleep, roused only with significant physical stimulation.
    • Unarousable.

      • .Table 2: Apgar score (Simon et al., 2017) Score 0 points 1 point 2 points Appearance (Skin color) Cyanotic / pale all over Peripheral cyanosis only. Pink Pulse (Heart rate) 0 \<100 100-140 Grimace (Reflex irritability) No response to stimulation Grimace or weak cry when stimulated Cry when stimulated Activity (Tone) Floppy Some flexions Well flexed and resisting extension Respiration Apneic Slow, irregular Strong cry

VI. Study outcomes:

  1. Primary outcome:

    a) the incidence of shivering attacks intraoperative. ( using Bedside Shivering Assessment Scale)

  2. Secondary outcomes:

    1. Apgar score at 1 and 5 minutes, Apgar is a quick test performed on a baby at 1 and 5 minutes after birth. The 1-minute score determines how well the baby tolerated the birthing process. The 5-minute score tells the health care provider how well the baby is doing outside the mother's womb. It also helps measure how well the baby responds if resuscitation is needed right after birth.
    2. Intraoperative hemodynamics assessment Immediately after injection of the medications and every 10 minutes till the end of the procedure including: heart rate, arterial blood pressure and number of hypotensive episodes
    3. Sedation of the mother immediately after injection of drug and after 30 minutes using The University of Michigan Sedation Scale (UMSS)
02

Conditions studied

  • Intraoperative Shivering
  • Ketamine With Shivering
  • Dexamethasone for Shivering
  • Severe Shivering

Keywords

  • shivering
  • ketamine
  • dexamethasone
03

In context

Lead sponsor

Kasr El Aini Hospital is the lead sponsor of 273 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

    1. Inclusion criteria

      • pregnant females
      • aged 18 to 45 years
      • ASA physical status II
      • elective Cesarean sections under spinal anesthesia

        1. Exclusion criteria
      • Contraindications for spinal anesthesia
      • Emergency cesarean sections
      • Patient with initial body temperature >38°c or \<36°c
      • Allergy to any of the drugs used in the study
      • Pre Existing neurological diseases (particularly those that wax and wane, e.g.multiple sclerosis)
      • Thrombocytopenia and coagulation disorders.
      • Severe stenotic heart disease.

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
110 participants (actual)

Study arms

  • Active comparator
    ketamine group

    Group K (ketamine): syringe (1): the ketamine syringe, dilute 25 mg ketamine in 10 ml saline to have a concentration of 2.5mg/ml. The dose will be 0.25 mg/kg, so we will give 0.1ml/kg of the syringe. syringe (2): saline syringe 10 ml saline in 10 ml syringe. (for double blinded technique). we will give 0.1ml/kg of the syringe.

    Drug: Ketamine Hydrochloride

  • Active comparator
    ketamine dexamethasone group

    Group KD (ketamine plus dexamethasone): Syringes (1): the ketamine syringe, dilute 25 mg ketamine in 10 ml saline to have a concentration of 2.5mg/ml. The dose will be 0.25 mg/kg, so we will give 0.1ml/kg of the syringe. Syringe (2): dexamethasone syringe, 10 mg dexamethasone will be diluted with 10 ml saline in 10 ml syringe, concentration will be 1mg/ml. the dose will be 0.1 mg/kg, so we will give 0.1ml/kg of the syringe.

    Drug: Ketamine Hydrochloride

Interventions

  • DrugKetamine Hydrochloride

    intravenous injection

    Also known as: dexamethasone

06

What researchers measure

Primary outcomes

  1. number of shivering episodes

    ● the number of shivering episodes scored ≥3 will be recorded.

    Time frame: the whole procedure and for 60 minutes postoperative

Secondary outcomes

  1. sedation score of the mother

    Time frame: 120 minutes

  2. APGAR score of the baby

    Time frame: 5 minutes

  3. hemodynamics

    Time frame: 120 minutes

07

Study locations

1 site
  • Kasr Al Aini Hospitals
    Cairo, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06091657
Lead sponsor
Kasr El Aini Hospital
Responsible party
Amany Ahmed Eissa (lecturer of anesthesia& ICU, Kasr El Aini Hospital) — Principal investigator
First posted
Oct 19, 2023
Start date
Jan 1, 2024
Primary completion
Jul 15, 2024
Completion
Jul 30, 2024
Last update
Jan 17, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion