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Dexamethasone in Prolonging the Duration of Spinal Anesthesia Among Pregnant Patients

Role of Intravenous Dexamethasone in Prolonging the Duration of Sub-Arachnoid Block in Pregnant Patients Undergoing Lower Segment Cesarean Section

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07088146
Enrollment
110
Registered
2025-07-28
Start date
2025-07-20
Completion date
2025-10-20
Last updated
2025-07-28

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

Conditions

Post Operative Analgesia, Spinal Anesthesia

Keywords

Adjuvants, Sub-Arachnoid Block, C-section

Brief summary

Lower segment C section is one of the most commonly performed surgeries worldwide. It is performed in spinal anesthesia. During Spinal Anesthesia a local anesthetic drug is administered in a space surrounding spinal cord and it blocks nerves originating from spinal cord providing both anesthesia and analgesia. This technique avoids harmful exposure of drugs to the baby inside the womb of mother. However this technique provides anesthesia and analgesia of limited duration which can be prolonged by addition of drugs to patient management regimen. One such drug is Dexamethasone which is a steroid commonly administered in the peri-operative period.

Detailed description

To prolong the duration of Sub-Arachnoid block number of drugs which are known as adjuvants can be used. One of the commonly used adjuvant is Dexamethasone a steroid given by intravenous route having anti-emetic and anti-inflammatory effect. This drug also prolongs the duration of Sub-Arachnoid block which can be helpful in case of lengthy surgical procedure and also extends the duration of analgesia in the post operative period.

Interventions

DRUGDexamethasone

Immediately after sub-arachnoid block 8mg of Dexamethasone will be administered intravenously

DRUGPlacebo

2ml of Normal saline will be given intravenously immediately after administration of spinal anesthesia

Sponsors

Rawalpindi Medical College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* American Society of Anesthesiologists (ASA) class: II and above. * Elective Cesarean section under Spinal Anesthesia.

Exclusion criteria

* Gestational diabetes * Body mass index \>35 kg/m2 * Diabetes mellitus * Adrenal insufficiency * Chronically receiving steroids * Allergic to study medications * Sensory block level less than T4

Design outcomes

Primary

MeasureTime frame
Time for block to regress by two dermatomes in post operative periodThis will be the time in minutes from end of C section in post operative period for the block to regress by two dermatomes

Secondary

MeasureTime frame
Time to rescue analgesiaThis will be the time in minutes from the end of Cesarean section in the post operative period to first rescue analgesia.

Countries

Pakistan

Contacts

Primary ContactHuda Tariq, MBBS
Huda8829@gmail.com+92-321-8829413

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026