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Impact of patient - controlled analgesia on patient's satisfaction after cardiac surgery in Shahid Rajaei Heart center in 2011.

Impact of patient - controlled analgesia on patient's satisfaction after coronary artery bypass surgery in Shahid Rajaei Heart center in 2011.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103195665N2
Enrollment
Unknown
Registered
2011-07-20
Start date
2011-08-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

pain control after heart surgery. Other post procedural disorders of circulatory system, not elsewhere classified

Interventions

Intervention 1: The interventional group, to be trained using Patient Control Analgesia (PCA=Patient Control Analgesia pump).In this method during two days post surgery, the physician determines the t
Treatment - Devices
Treatment - Drugs
The interventional group, to be trained using Patient Control Analgesia (PCA=Patient Control Analgesia pump).In this method during two days post surgery, the physician determines the type and paramete
In control group the pain will control by the nurse (Nurse Control Analgesia) as usual and routine of unit, based on physician orders, during two days postoperatively. During two days the satisfacti

Sponsors

Tabriz Medical Science University, Vice chancellor for research, Dr. Mohamreza Rashidi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 30-60 years old; admission in cardiac surgery ICU for bypass surgery; consent for participation in research Exclusion criteria: to have addiction; sensitivity for Morphine; not to be able for working with patient control anesthesia; renal diseases with creatine more than2; liver disease; to have re surgery for bleeding; psychological disease; unstable hemodynamic status with blood presser less than 90 mmHg, and receiving inotrope medications; low consciousness; ejection fraction less than %30;entrance to operating room by emergency; intubation more than 6 hours.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient satisfaction of pain control. Timepoint: every 12 hours after heart surgery until 2 days after surgery. Method of measurement: Pain Treatment Satisfaction Scale.

Secondary

MeasureTime frame
Nurses opinions about pain control method. Timepoint: every 12 hours after heart surgery until 2 days postsurgery. Method of measurement: by 6 questions about nurses opinions.;Pain Severity. Timepoint: Every 4 hours for 2 days after surgery. Method of measurement: Visual Analog Scale.;Sedation level. Timepoint: Every 4 hours for 2 days after surgery. Method of measurement: Sedation Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtoosa Hosseinzade

Tabriz Medical Science University

Atoosa.Hosseinzaeh@yahoo.com+98 41 1477 0648

Outcome results

None listed

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