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Comparative study on the effect of adding Dexmedetomidine than intrathecal Marcaine than Sufentanil in elective cesarean surgery

Comparative study on the effect and non effect of adding Dexmedetomidine than intrathecal Marcaine than Sufentanil in elective cesarean surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101814333N82
Enrollment
60
Registered
2017-10-25
Start date
2017-11-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

wound cesarean. Maternal care due to uterine scar from previous surgery

Interventions

Intervention 1: The first intervention group will receive 5 mg / d of Dexmedetomidine and 10 mg of Hyperbaric marcaine 0.5%. Intervention 2: The second intervention group will receive 5mg of sufentani
Treatment - Drugs
The first intervention group will receive 5 mg / d of Dexmedetomidine and 10 mg of Hyperbaric marcaine 0.5%.
The second intervention group will receive 5mg of sufentanil with 10mg of hyperbaric marcaine 0.5%

Sponsors

Vice chancellor for research, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: singleton, 18 to 45 years term pregnant women with a body mass of 18 to 30 with ASA class 1 candidate for cesarean section Exclusion criteria: Having any underlying disease such as cardiovascular disease (IHD cardiomyopathy), pre-eclampsia, Hypertension; neurological diseases such as migraine; Psychiatric diseases; History of allergy to local anesthesia; Emergency cesarean surgery; Cases requiring general anesthesia during surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Painless. Timepoint: At the time of 1, 2, 4, 6, 8, 10, 12, 16, 20 and 24 hours after the end of surgery. Method of measurement: Question from patient and visual observation (VAS).;Headache. Timepoint: At the time of 1, 2, 4, 6, 8, 10, 12, 16, 20 and 24 hours after the end of surgery. Method of measurement: Question from patient and visual observation (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahrokh Alikhani

Kermanshah University of Medical Sciences

parvizi.abfa@gmail.com+98 83 3427 6301

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026