Incidence of Spinal Anesthesia PreferenceNCT06910826
Visual Education for Spinal Anesthesia Acceptance
An observational study of Incidence of Spinal Anesthesia Preference, run by Istinye University at 1 site in Turkey (Türkiye).
Trial summary
Primary outcome: To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog. Secondary outcomes: To analyze independent (age, education, profession, previous experiences) and dependent (fear, anxiety) factors influencing patient choices. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women only
- Conditions the study is for
- Incidence of Spinal Anesthesia Preference
- How many people
- 318 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Apr 2025to 15 Aug 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 45 years
- Women only
- No healthy volunteers
- Adult
Study population: The study will include 318 pregnant women aged 18-45 who are undergoing elective cesarean sections and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale.
Who may be able to join
- Aged 18-45
- who are undergoing elective cesarean sections
- and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale
Who cannot join
- patients under 18 or over 45 years old,
- emergency cesareans,
- preeclampsia,
- cardiovascular disorders,
- fetal abnormalities,
- those not receiving spinal anesthesia or converted to general anesthesia during surgery,
Show all 9Show fewer
- those who refuse to participate in the study,
- hospital clinical or administrative staff,
- patients with psychiatric disorders
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
ilke dolgun contact
Turkey (Türkiye)1 site
Istinye Üniversity
Istanbul, Merkez Mahallesi, 34250
ilke dolgun, ilkeser2004@gmail.com
ilke dolgun
About this study
Official title: Explaining Spinal Anesthesia to Pregnant Women: A Visual Approach to Overcoming Fears
Primary outcome: To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog.
Secondary outcomes: To analyze independent (age, education, profession, previous experiences) and dependent (fear, anxiety) factors influencing patient choices.
What is being measured
The primary outcome is the main question the study is designed to answer.
incidence of spinal anesthesia preference
To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog
Measured: 4 MONTH
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2025
- Study start1 Apr 2025 (estimated)
- Primary completion1 Aug 2025 (estimated)
- Study completion15 Aug 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Incidence of Spinal Anesthesia PreferenceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 318 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Istinye University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, İlke Dolgun, Istinye University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06910826
- Sponsor's protocol ID
- haseki broşür
- Status last verified
- Mar 2025
- First submitted
- 28 Mar 2025
- Last updated
- 4 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Emadi SA, Gholipour Baradari A, Khademloo M, Abotorabi M, Hassanzadeh Kiabi F. Evaluating patients' choice of general and spinal anesthesia for elective cesarean section and associated factors: a descriptive study. Ann Med Surg (Lond). 2023 Jan 12;85(1):6-12. doi: 10.1097/MS9.0000000000000010. eCollection 2023 Jan.
PubMed 36742112Shahid N, Rashid AM. Knowledge, fear and acceptance rate of spinal anesthesia among pregnant women scheduled for cesarean section: a cross-sectional study from a tertiary care hospital in Karachi. BMC Anesthesiol. 2024 Nov 12;24(1):408. doi: 10.1186/s12871-024-02736-x.
PubMed 39533188
Study at a glance
From the registry record, last updated by the sponsor on 4 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Explaining Spinal Anesthesia to Pregnant Women: A Visual Approach to Overcoming Fears
- ClinicalTrials.gov ID
- NCT06910826
- Acronym / sponsor ID
- haseki broşür
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 318 participants (estimated)
- Lead sponsor
- Istinye UniversityUniversity, hospital or other
- Study start
- 1 Apr 2025 (estimated)
- Primary completion
- 1 Aug 2025 (estimated)
- Study completion
- 15 Aug 2025 (estimated)
- First posted
- 4 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Primary outcome: To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog.
Secondary outcomes: To analyze independent (age, education, profession, previous experiences) and dependent (fear, anxiety) factors influencing patient choices.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- The study will include 318 pregnant women aged 18-45 who are undergoing elective cesarean sections and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale.
Key inclusion criteria (3 listed)
- Aged 18-45
- who are undergoing elective cesarean sections
- and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale
Key exclusion criteria (9 listed)
- patients under 18 or over 45 years old,
- emergency cesareans,
- preeclampsia,
- cardiovascular disorders,
- fetal abnormalities,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
incidence of spinal anesthesia preference
Time frame: 4 MONTH
To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Apr 2025.
- Results publication: PubMed 36742112Emadi SA, Gholipour Baradari A, Khademloo M, Abotorabi M, Hassanzadeh Kiabi F. Evaluating patients' choice of general and spinal anesthesia for elective cesarean section and associated factors: a descriptive study. Ann Med Surg (Lond). 2023 Jan 12;85(1):6-12. doi: 10.1097/MS9.0000000000000010. eCollection 2023 Jan.
- Results publication: PubMed 39533188Shahid N, Rashid AM. Knowledge, fear and acceptance rate of spinal anesthesia among pregnant women scheduled for cesarean section: a cross-sectional study from a tertiary care hospital in Karachi. BMC Anesthesiol. 2024 Nov 12;24(1):408. doi: 10.1186/s12871-024-02736-x.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
ilke dolgun contact
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Incidence of Spinal Anesthesia Preference, run by Istinye University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 4 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact ilke dolgun (+905555485632, ilkeser2004@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
incidence of spinal anesthesia preference (time frame: 4 MONTH). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06910826, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Apr 2025.