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The Effect of Patient Preparation by Multimedia Method on Anxiety, Pain, and Consumption of analgesic after Vitrectomy surgery.

The Effect of Patient Preparation by Multimedia Method on Anxiety, Pain, and Consumption of analgesic after Vitrectomy surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180603039968N1
Enrollment
120
Registered
2018-10-10
Start date
2018-07-23
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

Anxiety

Interventions

Intervention 1: Study group: After selecting the block, the allocation of patients to the study group is determined. On the night before the surgery, by considering the entry requirements of the study

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: People's willingness to participate in the study Age range of 18 years old to 70 years old Hospitalization for at least 1 day before surgery No history of mental illness No prohibition of non-steroidal anti-inflammatory drugs and analgesics No addiction to drugs The patient should have the ability of seeing and hearing Patients who are candidates for single-eye vitrectomy surgery because of retinal detachment The patients will be placed in group I or group II according to the physical state of ASA

Exclusion criteria

Exclusion criteria: Inability to speak Non-Iranian nationality Any factor that leads the patient to become unresponsive after surgery Having the history of attending anxiety control and problem-solving training classes

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: The night before the operation and 30 minutes before entering the operating room. Method of measurement: Spielberger questionnaire.;Pain. Timepoint: In the recovery room before entering the department; 1,2,3,4 hours after entering the department. Method of measurement: VAS.;Consumption of analgesics. Timepoint: In the recovery room before entering the department; 1,2,3,4 hours after entering the department. Method of measurement: mg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEsmaeil Kargar

Shiraz University of Medical Sciences

esmaeil.kargarda@gmail.com+98 71 3629 1470

Outcome results

None listed

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