RecruitingPhase 4ketamine

Evaluation of Ketamine as Sedative Agent in Endoscopic Retrograde Cholangiopancreatography (ERCP)

Sponsored by Universiti Kebangsaan Malaysia Medical Centre

NCT ID
NCT04490031
Target Enrollment
140 participants
Start Date
2020-03-01
Est. Completion
2021-04-30

About This Study

This is a study evaluating the usage of Ketamine as sedative agent in ERCP. The usage of Ketamine will be compared to the standard sedation in our center, which is Midazolam in combination with Pethidine as analgesia.

Conditions Studied

Ketamine Adverse Reaction

Interventions

  • Ketamine Hydrochloride

Eligibility

Age:16 Years - N/A
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Malaysian citizens of who is able to give valid consent
* Patient planned for ERCP (either emergency or elective)

Exclusion Criteria:

* Known hypersensitivity towards Ketamine or Midazolam
* Patient refusal to participate or unable to give consent
* Increased intracranial pressure, acute stroke (\<3 months), intracranial haemorrhage (\<3 months)
* Uncontrolled hypertension (BP\>160/100) and tachycardia (Heart rate \>120)
* Acute myocardial infarction, acute coronary syndrome (\<3 months)
* Tachyarrythmia
* Pregnancy
* IVDU or substance abuse patient
* Patient with history of hallucination
* Child's Pugh Class C

Study Locations (1)

University Kebangsaan Malaysia Medical center
Bandar Tun Razak, Kuala Lumpur, Malaysia

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Muhammad Hafiz Ismail, MBBS
CONTACT
6016 3354384muhdhafizismail88@gmail.com
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

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Evaluation of Ketamine as Sedative Agent in Endoscopic Retrograde Cholangiopancreatography (ERCP) | Huxley