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Standardized Patient Education in Pituitary Surgery

The Impact of Standardized Patient Education on Patient Outcomes in Transsphenoidal Pituitary Surgery

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07618949
Enrollment
102
Registered
2026-06-01
Start date
2026-06-01
Completion date
2027-09-01
Last updated
2026-06-01

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

Conditions

Pituitary Adenoma

Keywords

Pituitary tumor, transsphenoidal surgery, Patient education

Brief summary

Protocols are being developed and implemented to ensure the best possible recovery process for patients undergoing transsphenoidal surgery, and their impact on patient outcomes is being evaluated. In studies where perioperative protocols-including patient education (verbal and written instruction on dehydration, hyponatremia, adrenal insufficiency, CSF leakage, meningitis, and the signs and symptoms of visual or other neurological disorders)-are implemented, it has been reported that patients' length of hospital stay is reduced, the rate of patients experiencing hyponatremia has decreased, and readmissions have declined (Sanchez-Garavito et al., 2024; Sarris et al., 2021). However, since these studies included protocols covering the entire surgical process-not just patient education-it is difficult to determine whether changes in patient outcomes stem from patient education or from alterations in other parameters within the protocol. Therefore, in the clinic where this study will be conducted, the effect of patient education on postoperative patient outcomes will be examined by developing an educational material that standardizes patient education, without making any changes to the surgical or pharmacological processes.

Interventions

OTHERStandardized Pituitary Training

The standardized educational material to be used with the training group was developed by the researchers through a literature review and includes evidence-based recommendations that patients should follow after pituitary surgery. The educational material and the sources used to create it are included in the appendix. Before providing education to patients in the intervention group, nurses and resident physicians working in neurosurgery will receive in-person training on the rationale and details of the material. Patients will be included in the education program starting from their preoperative hospital admission; the content of the educational material will be explained by a nurse, and a visual copy will be provided to both the patient and their caregiver. Additionally, the material will be posted in a clearly visible location in the patient's room.

Sponsors

Uludag University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Admitted for elective surgery due to a pituitary tumor. * Has not previously undergone surgery for the same medical condition. * Has voluntarily agreed to participate in the study. * Has no missing medical data. * Can speak Turkish or understand what is being explained. * Patients aged 18 and older.

Exclusion criteria

* Emergency surgery will be performed. * Revision surgery will be performed. * Those who voluntarily decline to participate in the study. * Those with incomplete medical data. * Those who cannot speak or understand Turkish. * Patients under the age of 18.

Design outcomes

Primary

MeasureTime frame
The total time from admission to discharge for patients who received standardized patient education in transsphenoidal pituitary surgery"From the registration phase through to the end of the 52-week training program"

Secondary

MeasureTime frame
Complication rates (meningitis, hyponatremia, CSF leak) and rates of unplanned readmission among patients who received standardized training in transsphenoidal pituitary surgery during their hospital stay.From the registration phase through to the end of the 52-week training program

Contacts

CONTACTAKİF BULUT, PhD
akifblt23@gmail.com+905468722872

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026