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Effect of deep and slow breathing on consequences of pain during arterial sheath removal in patients undergoing percutaneous coronary intervention

Effect of deep and slow breathing on consequences of pain during arterial sheath removal in patients undergoing percutaneous coronary intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050622120N1
Enrollment
60
Registered
2015-11-03
Start date
2015-10-23
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

Patients undergoing coronary angioplasty. Status following coronary angioplasty NOS

Interventions

Intervention 1: Patients in the intervention group admission is trained on how to take slow, deep breathing and 15 minutes before leaving again in terms of learning and doing clean properly controlle
Prevention
Patients in the intervention group admission is trained on how to take slow, deep breathing and 15 minutes before leaving again in terms of learning and doing clean properly controlled technique. To
In the control group, patients in the usual way and without the use of deep breathing and slow the sheet out.

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients in the study are that have these criteria: • For the first time undergoing coronary angioplasty, as well. • Have the ability to learn. • Has a mental disorder is not known, according to their relatives. • Fluency in Farsi and is able to communicate. • To participate in the study have written consent. • Systolic blood pressure is less than 130 mmhg. • any shortness of breath and breathing difficulties are clear. • The absence of pain and complication of vascular puncture to remove the sheet. Patients who have the following conditions shall be excluded: • Housing has received for any reason. • Experience shortness of breath, irregular heart disease, congestive heart failure or heart attack is. • Experiencing cardiac arrest is from respiratory or loss of consciousness. • Be deterred from continuing to study. • Fatal or transfer him to the operating room for emergency surgery any.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the intervention, immediately after the intervention, 10 and 20 minutes after intervention. Method of measurement: Pain visual scale.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before the intervention, immediately, 5,10,15,20 minutes later. Method of measurement: Digital Sphygmomanometer.;Pulse Rate. Timepoint: Before the intervention, immediately, 5,10,15,20 minutes later. Method of measurement: Cardiac monitoring.;Respiratory rate. Timepoint: Before the intervention, immediately, 5,10,15,20 minutes later. Method of measurement: Respiration monitoring.;Bleeding. Timepoint: Immediately after the homeostasis, 4 and 24 hours later. Method of measurement: Observation.;Hematoma. Timepoint: Immediately after the homeostasis, 4 and 24 hours later. Method of measurement: Observation and examination.;Pseudoaneurism. Timepoint: Immediately after the homeostasis, 4 and 24 hours later. Method of measurement: Observation and examination and sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Kobra Rahzani

Arak University of Medical Sciences

k.rahzani@yahoo.com+98 86 3313 6055

Outcome results

None listed

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