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Effect Of Pain Management On Physiological Parameters Of Patients after surgery

Comparative study on the effect of numerical pain assessment (systematic pain management) and pain control without using numerical criteria of pain on physiological indices in patients undergoing coronary artery bypass graft surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190213042695N1
Enrollment
56
Registered
2019-06-30
Start date
2019-06-21
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Patients undergoing coronary artery bypass graft surgery. Atherosclerosis of coronary artery bypass graft(s) and coronary artery of transplanted heart with angina pectoris

Interventions

Intervention 1: Intervention group: In the intervention group, the effect of assessing the intensity of pain using visual analogue scale (VAS) is examined every 30 minutes until 24 hours after surgery

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: All patients undergoing a coronary artery bypass graft surgery who are spending the first 24 hours following the extubation of the tracheal tube having complete consciousness Age of 30 to 75 years old Elective coronary artery bypass graft surgery Familiarity with Persian language and the ability to answer questions Hospitalization for at least 48 hours in intensive care unit

Exclusion criteria

Exclusion criteria: Experience of emergent coronary artery bypass graft surgery Hearing and speech problems Opiate and pain killers sensitivity Get tranquil or analgesic drugs, opiate and alcohol continuously Presence of underlying diseases (pulmonary disease, cancer, hepatitis, etc.) Inability to speak Persian and answer questions Use of coronary artery balloon pump during surgery Patients with permanent Pace maker Patients with electrolyte disturbances Patients with arthropathy and motor problems

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The first 24 hours after extubated and patient's complete alertness. Method of measurement: Numeric scale (Numerical measurement of pain).

Secondary

MeasureTime frame
Respiratory rate in one minute. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: Will be measured using monitoring.;SPO2. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: Will be measured using monitoring.;Heart rate in one minute. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: Will be measured using monitoring.;Temperature. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: It will be measured using a digital thermometer.;Systolic blood pressure. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: The blood pressure monitor will be monitored.;Diastolic blood pressure. Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: The blood pressure monitor will be monitored.;MAP (Median arterial pressure). Timepoint: The first 24 hours after the end of the tracheal tube will be measured every half hour. Method of measurement: It will be monitored and measured using intra-arterial catheters.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHomeira Soleymani Vafaii

Shahid Beheshti University of Medical Sciences

soleymani61@sbmu.ac.ir+98 21 7781 6477

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026