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A Low Dose Dexmedetomidine in Sedation Colonoscopy

Effect of Low-dose Dexmedetomidine on Hypotension in Colonoscopy:a Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06208956
Enrollment
104
Registered
2024-01-17
Start date
2024-01-20
Completion date
2024-02-29
Last updated
2024-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colonoscopy

Brief summary

104 patients who undergo painless colonoscopy from January 20,2024 to February 29,2024 will be randomized to two groups: propofol group and dexmedetomidine group. In the dexmedetomidine group,dexmedetomidine is infusion intravenously with a loading dose of 0.5 μg kg-1 for 10 min, then infusion at 0.3 μg kg-1 h-1 according to the ideal body weight of the patient until the end of colonoscopy. In the propofol group, Propofol is administrated 1 mg kg-1 intravenously, then titrated given by 0.5 mg kg-1 during the whole process.

Detailed description

104 patients who undergo painless colonoscopy from January 20,2024 to February 29,2024 will be randomized to two groups: propofol group and dexmedetomidine group. In the dexmedetomidine group,dexmedetomidine is infusion intravenously with a loading dose of 0.5 μg kg-1 for 10 min, then infusion at 0.3 μg kg-1 h-1 according to the ideal body weight of the patient until the end of colonoscopy. In the propofol group, Propofol is administrated 1 mg kg-1 intravenously, then titrated given by 0.5 mg kg-1.For all patients, if Ramsay sedation scale score reach 3, colonoscope will be inserted. During the whole process, maintenance Ramsay score of 3 to 4. Propofol 10 mg will be administrated as the rescue dose if body movement occur during colonoscopy. The primary outcome is the occurrence of hypotension. Key secondary outcomes are time-weighted average (TWA), area under the threshold (AUT) and cumulative duration of hypotension, as well as the maximum reduction in BP. Other secondary outcomes include(1) the incidence of bradycardia, hypoxemia or body movement;(2) discharge time (from the end of colonoscopy to discharge); (3) patients and endoscopists' satisfaction score (using an 11-point Likert scale, with 0 indicating very dissatisfied and 10 indicating very satisfied); (4) the incidence of dizziness, fatigue, or nausea and vomiting

Interventions

DRUGDexmedetomidine

In the dexmedetomidine group, dexmedetomidine is infusion intravenously with a loading dose of 0.5 μg kg-1 for 10 min, then infusion at 0.3 μg kg-1 h-1 according to the ideal body weight of the patient until the end of colonoscopy. During the whole process, maintenance Ramsay score of 3 to 4. Propofol 10 mg will be administrated as the rescue dose if body movement occur during colonoscopy.

DRUGPropofol

Propofol is administrated 1 mg kg-1 intravenously, then titrated given by 0.5 mg kg-1 until Ramsay score reach 3. During the whole process, propofol is given intermittently to maintain Ramsay score 3 to 4. If body movement happen, propofol 10mg will be administrated every time.

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients aged above 18 years 2. American Society of Anesthesiologists (ASA) physical status of 1-2 3. Patients scheduled for sedation colonoscopy

Exclusion criteria

1. Emergency patients 2. Body weight \< 40 kg or \>100 kg 3. Allergy to dexmedetomidine, propofol in this trail, a previous adverse reaction to dexmedetomidine or propofol 4. Pregnancy or lactation 5. Drug abusers 6. Participation in other clinical studies within the previous 3 months 7. renal impairment (glomerular filtration rate \< 60 ml/min), significant hepatic impairment (ascites, cirrhosis, or with international normalized ratio(INR) \>1.5)

Design outcomes

Primary

MeasureTime frameDescription
The primary outcome is the incidence of hypotensionThe time during colonoscopy, an average of 15 minutesHypotension is defined as 20% decrease from baseline systolic blood pressure (SBP) or diastolic blood pressure (DBP), or SBP \< 90, and/or DBP \< 50 mmHg

Secondary

MeasureTime frameDescription
Time-weighted average (TWA)The time during colonoscopy, an average of 15 minutesTWA is calculated as the AUT divided by the total duration of colonoscopy
Cumulative duration of hypotensionThe time during colonoscopy, an average of 15 minutesThe total time of patients experience hypotenion(hpotension defined as 20% decrease from baseline systolic blood pressure (SBP) or diastolic blood pressure (DBP), or SBP \< 90, and/or DBP \< 50 mmHg)
Maximum reduction in blood pressure (BP)The time during colonoscopy, an average of 15 minutesMaximum reduction in systolic blood pressure (SBP) ,diastolic blood pressure (DBP) and mean arterial pressure (MAP) from baseline
The incidence of bradycardiaThe time during colonoscopy, an average of 15 minutesBradycardia is defined as heat rate(HR) \<50 beats/min
The incidence of hypoxemiaThe time during colonoscopy, an average of 15 minutesHypoxemia is defined as oxygen saturation (SpO2)\<90%
The body movementThe time during colonoscopy, an average of 15 minutesThe twisting of the patient's body due to the stimulation of the colonoscopy, making it difficult to proceed with the procedure
Area under the threshold (AUT) of hypotensionThe time during colonoscopy, an average of 15 minutesAUT=depth of hypotension below (a 20% decrease in baseline SBP or DBP) or (90 mm Hg of SBP or 50 mm Hg of DBP)× time in minutes spent of hypotension. As an example, a patient undergoes colonoscopy that lasts 15 min, in which he experiences 2 episodes of hypotension, all lasting for 1 min and all with a minimal SBP of 80 mm Hg. The AUT = 2 min × (90 -80= 10 mm Hg under the SBP threshold of 90 mm Hg) = 2×10 = 20 mm Hg per minute.
Patients satisfaction scoreWhen the patient is fully awake after colonoscopy,an average of 5 minutesUsing an 11-point Likert scale, with 0 indicating very dissatisfied and 10 indicating very satisfied
Endoscopists'satisfaction scoreAt the end of colonoscopy,an average of 15 minutesUsing an 11-point Likert scale, with 0 indicating very dissatisfied and 10 indicating very satisfied
The incidence of dizzinessFrom the end of colonoscopy to discharge,an average of 40 minutesThe investigators consider it dizziness if patients fell any dizziness
The incidence of fatigueFrom the end of colonoscopy to discharge,an average of 40 minutesThe investigators consider it fatigue if patients fell any fatigue
The incidence of nausea and vomitingFrom the end of colonoscopy to discharge,an average of 40 minutesThe investigators consider it nausea and vomiting if patients fell any nausea and vomiting
Discharge timeFrom the end of colonoscopy to discharge,an average of 40 minutesFrom the end of colonoscopy to discharge

Contacts

Primary ContactLi Zhou
zlmz@wchscu.cn18980606160
Backup ContactMao Ye
838915882@qq.com13540432883

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026