Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:11 AM
Ignite Modification Date:
2025-12-25 @ 2:11 AM
NCT ID:
NCT05726760
Eligibility Criteria:
Inclusion Criteria:
* Full term (37-42 weeks) parturients
* ASA 1 and 2
* Singleton pregnancy
* Normal placental position
* Scheduled for category 4 LSCS
* 'Single-shot' spinal anaesthesia
* Signed informed consent
* Received a patient information leaflet
Exclusion Criteria:
* Any medical conditions that may affect peripheral temperature
* Parturients converted to other forms of anaesthesia (not just spinal anaesthesia)
* Parturients with a pyrexia / sepsis
* Parturients with peripheral vascular disease (including Raynauds)
* Parturients with cardiovascular disease
* Parturients with diabetes mellitus (gestational, type 1 or 2)
* Parturients with hypertensive disorders of pregnancy
* ASA 3+ Parturients
* BMI \>40 or \<18
* Parturient refusal.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
60 Years
Study:
NCT05726760
Study Brief:
Protocol Section:
NCT05726760