The Effect of Different Altitude Levels on Spinal Anesthesia in Cesarean Section Surgery (altitude)

May 7, 2024 updated by: Dilek Yeniay, Giresun University

The Effect of Different Altitude Levels on Spinal Anesthesia in Cesarean Section Surgery; Comparison of Anesthesia Parameters and Hemodynamic Changes

The aim of the researchers in this prospective study is to determine the differences, if any, in terms of anesthetic parameters among pregnant women who live at different altitudes and undergo cesarean section under neuraxial anesthesia under elective conditions and to contribute to the literature.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Increased intra-abdominal pressure during pregnancy increases the pressure in the epidural and spinal space and causes enlargement of the epidural veins. This may lead to easier increases in the anesthetic blockage level. For this reason, it is necessary to use the lowest possible dose of local anesthesia in these individuals compared to normal healthy individuals.

The literature on the effect of altitude difference on central neuraxial block is limited. Based on studies showing changes in CSF volume and content in hypoxic conditions, According to the researchers, with the same amount of local anesthetic, the duration of sensory and motor blockade at sea level is thought to be equal to or longer than in mid-high regions.

This study will be carried out among pregnant women who live in the city center at 3 different altitudes [0-10 m (Giresun), 810 m (Çorum), 1725 m (Van)] and undergo cesarean section under elective conditions. It will be performed in a multicenter, prospective, controlled, randomized manner in order to determine the differences, if any, among these pregnant women in terms of anesthetic parameters.

Study Type

Interventional

Enrollment (Actual)

150

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Giresun, Turkey
        • Gıresun gynecology and children's hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18-40 years old
  • Pregnant women 160-170 centimeters tall
  • Be residing in the place of participation for at least 1 month

Exclusion Criteria:

  • >ASA 2 pregnant women
  • Contraindicated for spinal anesthesia, such as infection or coagulation disorder at the needle insertion site
  • Pregnant women to be taken under emergency conditions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: sea levelaltitude
Pregnant women living in Giresun(sea levelaltitude),Turkey and undergoing cesarean section under elective conditions.
The same anesthesia protocol will be applied to the patient group at each altitude. In the sitting position, the spinal space was entered with a 25 gauge Quincke-tipped needle from the L4-5 space and a drop of CSF will be dripped onto the pH paper. Immediately afterwards, 12 mg of 0.5% hyperbaric bupivacaine will be given. The color formed on the pH paper will be noted. Sensory block level will be tested with pinprick test and motor block level will be evaluated with Modified Bromage scale. The number and duration of spinal anesthesia applications, the time of occurrence of sensory block in the T6 dermatome, the time to reach each score of the MB scale, the duration of the operation, the highest level of sensory block and anesthetic complications will be recorded. Sensory block time and motor block time of the patients followed in the service will be recorded.
Other Names:
  • sea level altitude, moderate altitude, high altitude
Active Comparator: moderate altitude
Pregnant women living in Çorum(moderate altitude),Turkey and undergoing cesarean section under elective conditions.
The same anesthesia protocol will be applied to the patient group at each altitude. In the sitting position, the spinal space was entered with a 25 gauge Quincke-tipped needle from the L4-5 space and a drop of CSF will be dripped onto the pH paper. Immediately afterwards, 12 mg of 0.5% hyperbaric bupivacaine will be given. The color formed on the pH paper will be noted. Sensory block level will be tested with pinprick test and motor block level will be evaluated with Modified Bromage scale. The number and duration of spinal anesthesia applications, the time of occurrence of sensory block in the T6 dermatome, the time to reach each score of the MB scale, the duration of the operation, the highest level of sensory block and anesthetic complications will be recorded. Sensory block time and motor block time of the patients followed in the service will be recorded.
Other Names:
  • sea level altitude, moderate altitude, high altitude
Active Comparator: high altitude
Pregnant women living in Van(high altitude),Turkey and undergoing cesarean section under elective conditions.
The same anesthesia protocol will be applied to the patient group at each altitude. In the sitting position, the spinal space was entered with a 25 gauge Quincke-tipped needle from the L4-5 space and a drop of CSF will be dripped onto the pH paper. Immediately afterwards, 12 mg of 0.5% hyperbaric bupivacaine will be given. The color formed on the pH paper will be noted. Sensory block level will be tested with pinprick test and motor block level will be evaluated with Modified Bromage scale. The number and duration of spinal anesthesia applications, the time of occurrence of sensory block in the T6 dermatome, the time to reach each score of the MB scale, the duration of the operation, the highest level of sensory block and anesthetic complications will be recorded. Sensory block time and motor block time of the patients followed in the service will be recorded.
Other Names:
  • sea level altitude, moderate altitude, high altitude

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
age
Time Frame: preoperative period
18-40 age frame
preoperative period
Body max index
Time Frame: preoperative period
kg/m2
preoperative period
heart rate
Time Frame: during the surgery
beats/min
during the surgery
American Society of Anesthesiologists (ASA)
Time Frame: preoperative period
ASA I and II
preoperative period
mean arterial pressure
Time Frame: during the surgery
mmHg
during the surgery
The number and duration of spinal anesthesia applications
Time Frame: during the surgery
second
during the surgery
the duration of sensory block formation in the T6 dermatome
Time Frame: during the surgery
second
during the surgery
the time to reach each score of the MB(Modified bromage scale) scale 1-2-3
Time Frame: during the surgery
second
during the surgery
the duration of the operation (time from the beginning of the surgical incision to the completion of the surgery)
Time Frame: during the surgery
minute
during the surgery
the highest level of sensory block
Time Frame: during the surgery
dermatome level
during the surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
postoperative block parameters
Time Frame: postoperative first 24 hour
Sensory block time (DBS) (time from local anesthetic injection until S2 dermatome sensation), motor block time (MBS) (time from local anesthetic injection to full motor function recovery) will be evaluated for the patients followed in the service.
postoperative first 24 hour
postoperative headache parameter
Time Frame: postoperative first and 7. day
On the first and seventh days after the operation, the patients will be questioned by the researcher for post-dural puncture headache (PDPH, increased pain intensity when standing up from the supine position) by phone call.
postoperative first and 7. day
postoperative nausea and vomiting parameter
Time Frame: postoperative first 24 hour
the degree of postoperative nausea and vomiting will be checked (Verbal Descriptive Scale).
postoperative first 24 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Dilek Yeniay, Giresun Universıty TURKEY

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2023

Primary Completion (Actual)

March 28, 2023

Study Completion (Actual)

April 15, 2023

Study Registration Dates

First Submitted

November 28, 2022

First Submitted That Met QC Criteria

January 27, 2023

First Posted (Actual)

February 8, 2023

Study Record Updates

Last Update Posted (Actual)

May 8, 2024

Last Update Submitted That Met QC Criteria

May 7, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • DYeniay

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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