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A Warmer Temperature Decrease Propofol Injection Pain

A Warmer Room-temperature at 27-28 Centi-degree Will Decrease Propofol Injection Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03420560
Enrollment
120
Registered
2018-02-05
Start date
2018-02-28
Completion date
2018-04-30
Last updated
2018-02-05

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

Conditions

Injection Site Irritation, Propofol Syndrome, Temperature Change, Body

Brief summary

Propofol injection pain will be surfed by up to 70-80 percentage by the Patients who induced by propofol. Temperature of Operating room was set to a certain range in normal clinical practice, which is 22- 26 centigrade. Warm feeling will make skin vassal dilated and more blood will pass through to bring more heat out of our body. It had been reported that a bigger venous vessels will get less propofol injection pain. The investigators hypothesis that Patients who stayed in a warmer room temperature will surf less injection pain while compare to a normal setting room temperature.

Interventions

Patients before general anesthesia induction will send to warmer operation Injection pain was accessed with (Visual analogous scale)VAS.

Sponsors

Xingui Dai
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Patients will not knowing the exact temperature of the room,thought they will have their own feeling about it. Data was collecting with a anesthesia nurse who do not know what will do with these data. data were assessed to an anesthesiologist who did not know the Group allocation.

Intervention model description

patients for observation will sent to a warmer operating room,while Patients in controled Group will send to normal setting operating room at about 23 centigrade.

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* ASA I\ III, aged 18,scheduled or emergency surgery with general anesthesia.

Exclusion criteria

* a history of allergy to propofol, allergy to soybean oil * with peripheral blood diseases.

Design outcomes

Primary

MeasureTime frameDescription
intensity of injection pain3 monthsintensity of injection pain was reported by patient themselves before loss their awareness.
numbers of lidocaine rescues for severe injection pain3 monthswhen unbearable injection happens,patient could ask for stop and 20mg lidocaine was injected as rescue treatments.
incidences of injection pain3 monthsNumeric Visual Analog Scale of injection \>2 was counted as injection pain happens,the total incidence of injection was compared in two groups.

Countries

China

Outcome results

None listed

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