18-45 Range of AgeNCT05624671
Is Elective Caesarean Sections for Predicting Post-spinal Hypotension Role of Overactive Bladder?
A study testing bupivacaine,fentanyl in people with 18-45 Range of Age and Cesarean Section, run by Ataturk University at 1 site in Turkey (Türkiye).
Trial summary
It is to predict postspinal hypotension that may develop in patients diagnosed with overactive bladder who will undergo elective cesarean section under spinal-epidural anesthesia. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- 18-45 Range of Age, Cesarean Section, Primigravid
- What is being tested?
- bupivacaine,fentanyl
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 143 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Aug 2019to 30 Dec 2021
- Phase
- Interventional
- Are there results?
- None posted in the registry
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
- Healthy volunteers accepted
- Adult
Who may be able to join
- ASA I-II
- Primigravid
- Elective cesarean sections
Who cannot join
- ≤18 age
- ≥45 age
- Emergency surgery
- Pregnancy-induced hypertension,
- Significant systemic disease,
- Multiple pregnancy,
Show all 11Show fewer
- Fetal or placental abnormality,
- History of hypersensitivity or allergy to drugs to be used in the study,
- Morbidly obese (BMI≥40),
- Patients for whom neuraxial anesthesia is contraindicated,
- Unable or unwilling to participate
Trial locations and contacts
1 site in 1 country.
About this study
It is to predict postspinal hypotension that may develop in patients diagnosed with overactive bladder who will undergo elective cesarean section under spinal-epidural anesthesia.
Read the detailed description
INTRODUCTION
Spinal anesthesia is the most preferred standard anesthesia technique in caesarean sections. After a C-section, hypotension develops in approximately 70% of pregnant women and 33% of nonpregnant women and this situation is generally more severe and sudden in pregnant women. Aortocaval compression and low basal vasomotor tone caused by the Gravid Uterus and sympathetic blockade associated with spinal anesthesia contribute to this sudden onset and deep hypotension. Serious post-spinal hypotension that is not properly treated can increase the risks of maternal and fetal complications. It is important to identify patients at high risk of developing hypotension. Because it will enable us to manage the process more proactively.
Many predictive methods such as thoracic electrical bioimpedance, heart rate (HR) variability, pupillary light reflex analysis, and perfusion index (PI) were used to predict the onset of hypotension. In some studies, it has been shown that hypotension may develop with disruption of the balance between sympathetic and parasympathetic nervous systems in the autonomic nervous system.
The bladder is an organ in which the sympathetic and parasympathetic system works in coordination. For a normal micturition, the balance between the sympathetic and parasympathetic systems should not be disturbed. Overactive bladder (OAB) is a syndrome that includes symptoms such as sudden and severe urination, urge to urinate suddenly, incontinence before reaching the toilet, and frequent urination (≥8 per day). Overactive bladder can be diagnosed based on subjective symptoms instead of urodynamic tests. In our country, the rate is 20% for males, 35.7% for females and 29.3% for both sexes. The main problem here is the balance disturbed between the sympathetic and parasympathetic systems.
Our primary goal in the study is to predict post-spinal hypotension that may develop in patients with a diagnosis of the overactive bladder who will undergo elective cesarean under combined spinal epidural anesthesia.
MATERIALS AND METHODS
These randomized triple-blind prospective studies will be performed on the primiparous pregnant woman in ASA I-II, 2nd and 3rd trimester, who will undergo an elective caesarean under combined spinal epidural anesthesia after obtaining informed written consent from patients and the ethics office of Medicine Research Hospital of Atatürk University. Exclusion criteria: ≤18 or ≥45 years of age, emergency obstetric surgery, pregnancy-induced hypertension, significant systemic disease, multiple pregnancy, fetal or placental abnormality, hypersensitivity or allergy history to drugs to be used in the study, morbid obesity (BMI≥40), autonomic neuropathy, diabetes, patients with contraindications to neuraxial anesthesia, multigravida, urinary tract infection, and Cre≥1.2, who are unable or unwilling to participate in the study will be excluded. Patients diagnosed with OAB will be classified as Group I and other patients will be classified as Group II. Patients will be randomly assigned to Group I and Group II. For this, a random number table will be used.
ANESTHESIC MANAGEMENT
After patients have transferred to the operation room, an intravenous (iv) access is obtained with an applicator size of 20, and routine monitorization consisting of electrocardiogram (ECG), peripheral oxygen saturation (SpO2), and non-invasive blood pressure is performed. While the patient is in the supine and lateral tilt positions, blood pressure and heart rate will be measured 2 times consecutively and the average of these values will be recorded as a baseline value. From the beginning of spinal anesthesia to the end of surgery Isolyte S will be infused at room temperature with 10 mL/kg / h speed to patients. According to our institutional protocol, intravenous (iv) hydration will not be given as preload, and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle, and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle. Blankets will be used to maintain the body temperature of patients and all fluids used during surgery will be delivered at 24 ° C. Oxygen will be given to patients at 4l / min with a face mask throughout the operation.
OVERACTIVE BLADDER DIAGNOSIS
The presence of OAB for each patient in the primipara who applied in the second and third trimesters will be determined using the Turkish version of OAB-V8, which consists of eight questions that can be graded on a 6-point scale ranging from 0 to 5; 0 (not at all), 1 (a little bit), 2 (somewhat), 3 (quite a bit), 4 (a great deal) and 5 (a very great deal). The lowest total score will be 0, the highest total score will be 40, and those with a higher score than 11 will be evaluated in favor of OAB. With the OAB-V8 form, a non-invasive uroflowmetry test will be applied to pregnant women, and tower-like diagram will be interpreted in favor of OAB.
STUDY PROTOCOLS
After the spinal anesthesia has been performed in the following first 10 minutes blood pressure and heart rate will be measured in every minute after the first 10 minutes will be measured in every 2.5 minutes until the baby is born. Hypotension will be defined as symptom complaints compatible with hypotension (ex: paleness, dizziness, shortness of breath, nausea or vomiting) without the systolic blood pressure falling below 20% or systolic blood pressure below 20% of the basal value. If hypotension occurs, it will be treated with ephedrine until blood pressure reaches baseline (initial dose 10 mg, intravenously) and rapid colloid or crystalloid infusion. If hypotension persists or recurs, vasopressor treatment will be repeated every 1 minute. Bradycardia will be described as having a heart rate of 50 beats/min and will be treated with 1mg iv atropine. The spinal anesthesia will be considered as unsuccessful if the sensorial block level has not reached the T6 level before surgery or felt pain during skin incision. In this case, 10 ml of 15 ml 2% lidocaine + 2 ml bicarbonate + 2 ml fentanyl + 1ml 1/200000 adrenaline solution will be given via epidural catheter and the patient will be excluded from the study. However, if pain felt again, will switch to general anesthesia. Post-spinal hypotension will be recorded from the onset of spinal anesthesia to the birth of the fetus. After the completion of the C-section, the time until the skin incision, uterine incision and time of birth, and the height, weight, BMI, and trimester of patients will be recorded. After the birth of the fetus, the study will be terminated and the total dose of ephedrine, adrenaline, and atropine used, as well as the amount of crystalloid, and colloid administered, and blood loss will be recorded. The study was triple-blind because the researchers who detected, recorded, and treated post-spinal hypotension did not know the results obtained from urological measurements and did not know about the groups analyzed by the statistician.
STATISTICAL ANALYSIS
Power analysis : Patients diagnosed with OAB are 15% more likely to develop hypotension than patients who do not receive this diagnosis. In order for a difference of 15% to be statistically significant, it was calculated by the PAS statistics program, which requires a total of 142 patients to be included in the study, where 71 patients should be in each group at a 95% confidence level at 80% power.
The analyzes were done with IBM SPSS 20 statistical analysis program.
Data were presented as mean, standard deviation, median, minimum, maximum, percentage, and number. The normal distribution of continuous variables was evaluated with the Shapiro Wilk-W test when the sample size was <50 and the Kolmogorov-Smirnov test when it was> 50.
In the comparisons between two independent groups, the Independent Samples t test was used when the normal distribution condition was met and the Mann Whitney u test was used when it was not provided.
In 2x2 comparisons between categorical variables, the expected value (> 5) was made using the Pearson Chi-square test, the expected value (3-5) was made using the chi-square yacht test and the expected value (<3) using Fisher's Exact test.
The statistical significance level was taken as p <0.05.
- Conditions
- 18-45 Range of Age, Cesarean Section, Primigravid
- Being tested
- bupivacaine,fentanyl
- Keywords
- cesarean section, spinal-epidural, overactive bladder, post-spinal hypotension
- Medical subject headings
- Urinary Bladder, Overactive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
bupivacaine,fentanylOther
According to our institution protocol, intravenous (iv) hydration will not be given as preload and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle.
| Study group | Role | What they receive |
|---|---|---|
| IS THERE ANY ROLE OF OVERACTIVE BLADDER IN POSTSPINAL HYPOTENSION IN ELECTIVE CAESAREAN SECTIONS? | Other | According to our institution protocol, intravenous (iv) hydration will not be given as preload and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle. Receives: Other: bupivacaine,fentanyl |
What is being measured
The primary outcome is the main question the study is designed to answer.
Is Elective Caesarean Sections for Predicting Post-spinal Hypotension (reduction of systolic blood pressure(mmHg) after spinal anesthesia) Role of Overactive Bladder?
It is to predict postspinal hypotension (systolic blood pressure below 20% of the basal value) that may develop in patients diagnosed with overactive bladder who will undergo elective cesarean section under spinal-epidural anesthesia.
Measured: Intraoperative period
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Nov 2022
- Study start1 Aug 2019
- Primary completion30 Dec 2021
- Study completion30 Dec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for 18-45 Range of AgeStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 143 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ataturk University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Aysenur Dostbil, Ataturk University
- Investigators
- AYŞENUR DOSTBİL, Study director, Ataturk University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05624671
- Sponsor's protocol ID
- B.30.2ATA.0.01.00/
- Status last verified
- Nov 2022
- First submitted
- 23 Sep 2022
- Last updated
- 22 Nov 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 22 Nov 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Is Elective Caesarean Sections for Predicting Post-spinal Hypotension Role of Overactive Bladder?
- ClinicalTrials.gov ID
- NCT05624671
- Acronym / sponsor ID
- B.30.2ATA.0.01.00/
- Conditions
- 18-45 Range of Age, Cesarean Section, Primigravid
- Keywords
- cesarean section, spinal-epidural, overactive bladder, post-spinal hypotension
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 143 participants (actual)
- Lead sponsor
- Ataturk UniversityUniversity, hospital or other
- Study start
- 1 Aug 2019 (actual)
- Primary completion
- 30 Dec 2021 (actual)
- Study completion
- 30 Dec 2021 (actual)
- First posted
- 22 Nov 2022 (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.
It is to predict postspinal hypotension that may develop in patients diagnosed with overactive bladder who will undergo elective cesarean section under spinal-epidural anesthesia.
Detailed description
INTRODUCTION
Spinal anesthesia is the most preferred standard anesthesia technique in caesarean sections. After a C-section, hypotension develops in approximately 70% of pregnant women and 33% of nonpregnant women and this situation is generally more severe and sudden in pregnant women. Aortocaval compression and low basal vasomotor tone caused by the Gravid Uterus and sympathetic blockade associated with spinal anesthesia contribute to this sudden onset and deep hypotension. Serious post-spinal hypotension that is not properly treated can increase the risks of maternal and fetal complications. It is important to identify patients at high risk of developing hypotension. Because it will enable us to manage the process more proactively.
Many predictive methods such as thoracic electrical bioimpedance, heart rate (HR) variability, pupillary light reflex analysis, and perfusion index (PI) were used to predict the onset of hypotension. In some studies, it has been shown that hypotension may develop with disruption of the balance between sympathetic and parasympathetic nervous systems in the autonomic nervous system.
The bladder is an organ in which the sympathetic and parasympathetic system works in coordination. For a normal micturition, the balance between the sympathetic and parasympathetic systems should not be disturbed. Overactive bladder (OAB) is a syndrome that includes symptoms such as sudden and severe urination, urge to urinate suddenly, incontinence before reaching the toilet, and frequent urination (≥8 per day). Overactive bladder can be diagnosed based on subjective symptoms instead of urodynamic tests. In our country, the rate is 20% for males, 35.7% for females and 29.3% for both sexes. The main problem here is the balance disturbed between the sympathetic and parasympathetic systems.
Our primary goal in the study is to predict post-spinal hypotension that may develop in patients with a diagnosis of the overactive bladder who will undergo elective cesarean under combined spinal epidural anesthesia.
MATERIALS AND METHODS
These randomized triple-blind prospective studies will be performed on the primiparous pregnant woman in ASA I-II, 2nd and 3rd trimester, who will undergo an elective caesarean under combined spinal epidural anesthesia after obtaining informed written consent from patients and the ethics office of Medicine Research Hospital of Atatürk University. Exclusion criteria: ≤18 or ≥45 years of age, emergency obstetric surgery, pregnancy-induced hypertension, significant systemic disease, multiple pregnancy, fetal or placental abnormality, hypersensitivity or allergy history to drugs to be used in the study, morbid obesity (BMI≥40), autonomic neuropathy, diabetes, patients with contraindications to neuraxial anesthesia, multigravida, urinary tract infection, and Cre≥1.2, who are unable or unwilling to participate in the study will be excluded. Patients diagnosed with OAB will be classified as Group I and other patients will be classified as Group II. Patients will be randomly assigned to Group I and Group II. For this, a random number table will be used.
ANESTHESIC MANAGEMENT
After patients have transferred to the operation room, an intravenous (iv) access is obtained with an applicator size of 20, and routine monitorization consisting of electrocardiogram (ECG), peripheral oxygen saturation (SpO2), and non-invasive blood pressure is performed. While the patient is in the supine and lateral tilt positions, blood pressure and heart rate will be measured 2 times consecutively and the average of these values will be recorded as a baseline value. From the beginning of spinal anesthesia to the end of surgery Isolyte S will be infused at room temperature with 10 mL/kg / h speed to patients. According to our institutional protocol, intravenous (iv) hydration will not be given as preload, and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle, and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle. Blankets will be used to maintain the body temperature of patients and all fluids used during surgery will be delivered at 24 ° C. Oxygen will be given to patients at 4l / min with a face mask throughout the operation.
OVERACTIVE BLADDER DIAGNOSIS
The presence of OAB for each patient in the primipara who applied in the second and third trimesters will be determined using the Turkish version of OAB-V8, which consists of eight questions that can be graded on a 6-point scale ranging from 0 to 5; 0 (not at all), 1 (a little bit), 2 (somewhat), 3 (quite a bit), 4 (a great deal) and 5 (a very great deal). The lowest total score will be 0, the highest total score will be 40, and those with a higher score than 11 will be evaluated in favor of OAB. With the OAB-V8 form, a non-invasive uroflowmetry test will be applied to pregnant women, and tower-like diagram will be interpreted in favor of OAB.
STUDY PROTOCOLS
After the spinal anesthesia has been performed in the following first 10 minutes blood pressure and heart rate will be measured in every minute after the first 10 minutes will be measured in every 2.5 minutes until the baby is born. Hypotension will be defined as symptom complaints compatible with hypotension (ex: paleness, dizziness, shortness of breath, nausea or vomiting) without the systolic blood pressure falling below 20% or systolic blood pressure below 20% of the basal value. If hypotension occurs, it will be treated with ephedrine until blood pressure reaches baseline (initial dose 10 mg, intravenously) and rapid colloid or crystalloid infusion. If hypotension persists or recurs, vasopressor treatment will be repeated every 1 minute. Bradycardia will be described as having a heart rate of 50 beats/min and will be treated with 1mg iv atropine. The spinal anesthesia will be considered as unsuccessful if the sensorial block level has not reached the T6 level before surgery or felt pain during skin incision. In this case, 10 ml of 15 ml 2% lidocaine + 2 ml bicarbonate + 2 ml fentanyl + 1ml 1/200000 adrenaline solution will be given via epidural catheter and the patient will be excluded from the study. However, if pain felt again, will switch to general anesthesia. Post-spinal hypotension will be recorded from the onset of spinal anesthesia to the birth of the fetus. After the completion of the C-section, the time until the skin incision, uterine incision and time of birth, and the height, weight, BMI, and trimester of patients will be recorded. After the birth of the fetus, the study will be terminated and the total dose of ephedrine, adrenaline, and atropine used, as well as the amount of crystalloid, and colloid administered, and blood loss will be recorded. The study was triple-blind because the researchers who detected, recorded, and treated post-spinal hypotension did not know the results obtained from urological measurements and did not know about the groups analyzed by the statistician.
STATISTICAL ANALYSIS
Power analysis : Patients diagnosed with OAB are 15% more likely to develop hypotension than patients who do not receive this diagnosis. In order for a difference of 15% to be statistically significant, it was calculated by the PAS statistics program, which requires a total of 142 patients to be included in the study, where 71 patients should be in each group at a 95% confidence level at 80% power.
The analyzes were done with IBM SPSS 20 statistical analysis program.
Data were presented as mean, standard deviation, median, minimum, maximum, percentage, and number. The normal distribution of continuous variables was evaluated with the Shapiro Wilk-W test when the sample size was <50 and the Kolmogorov-Smirnov test when it was> 50.
In the comparisons between two independent groups, the Independent Samples t test was used when the normal distribution condition was met and the Mann Whitney u test was used when it was not provided.
In 2x2 comparisons between categorical variables, the expected value (> 5) was made using the Pearson Chi-square test, the expected value (3-5) was made using the chi-square yacht test and the expected value (<3) using Fisher's Exact test.
The statistical significance level was taken as p <0.05.
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| IS THERE ANY ROLE OF OVERACTIVE BLADDER IN POSTSPINAL HYPOTENSION IN ELECTIVE CAESAREAN SECTIONS? | Other | Other: bupivacaine,fentanylAccording to our institution protocol, intravenous (iv) hydration will not be given as preload and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle. |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- ASA I-II
- Primigravid
- Elective cesarean sections
Key exclusion criteria (11 listed)
- ≤18 age
- ≥45 age
- Emergency surgery
- Pregnancy-induced hypertension,
- Significant systemic disease,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| bupivacaine,fentanylAccording to our institution protocol, intravenous (iv) hydration will not be given as preload and afterload and vasopressor infusion will not be initiated before spinal anesthesia. After the skin is prepared sterile and local infiltration with 2% lidocaine is done, from L3-L4 OR L4-L5 range on midline with the 16 gauge Tuohy needle and the loss of resistance technique epidural space is identified and then 26 gauge pencil point needle is passed trough the Touhy and the dura will be drilled. After the cerebrospinal fluid (CSF) is seen the fluid containing 5mg isobaric bupivacaine and 15µg fentanyl will be given in 30 seconds to patients. After the spinal needle is removed, the epidural catheter is placed 3-5 cm in the epidural space through Tuohy, and after the catheter is fixated, the patients will be placed in the supine position by placing a height under their right hip with a 15 ° angle. | Other | IS THERE ANY ROLE OF OVERACTIVE BLADDER IN POSTSPINAL HYPOTENSION IN ELECTIVE CAESAREAN SECTIONS? |
Primary outcome
Is Elective Caesarean Sections for Predicting Post-spinal Hypotension (reduction of systolic blood pressure(mmHg) after spinal anesthesia) Role of Overactive Bladder?
Time frame: Intraoperative period
It is to predict postspinal hypotension (systolic blood pressure below 20% of the basal value) that may develop in patients diagnosed with overactive bladder who will undergo elective cesarean section under spinal-epidural anesthesia.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Nov 2022.
- Individual participant dataSharing planned: Undecided
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. This study is not recruiting at the moment.
AYŞENUR DOSTBİL study director
Ataturk University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing bupivacaine,fentanyl in people with 18-45 Range of Age and Cesarean Section, run by Ataturk 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 11 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: finished, as of the sponsor's last update on 22 Nov 2022. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Is Elective Caesarean Sections for Predicting Post-spinal Hypotension (reduction of systolic blood pressure(mmHg) after spinal anesthesia) Role of Overactive Bladder? (time frame: Intraoperative period). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 22 Nov 2022; AzTrials last refreshed its copy on 27 Oct 2026.