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The effect of supplemental oxygen therapy on the rate of complications after cesarean surgery with Spinal anesthesia method in Besat hospital of Sanandaj

The effect of supplemental oxygen therapy on the incidence and severity of complications after cesarean surgery with spinal anesthesia method in educational and medical center of Besat-Sanandaj

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138806192440N1
Enrollment
120
Registered
2010-02-20
Start date
2009-11-21
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

the complications after caesarean surgery with the spinal anesthesia method. Delivery by caesarean section, unspecified

Interventions

Intervention 1: oxygen 60% equivalent to 10 liters per minute will be used during anesthesia and surgery and after surgery in recovery section for 6 hours using the Venturi mask. Intervention 2: In co
Treatment - Drugs
oxygen 60% equivalent to 10 liters per minute will be used during anesthesia and surgery and after surgery in recovery section for 6 hours using the Venturi mask
In control group routine care will be performed (oxygen 30% equivalent to 3-5 liters per minute)

Sponsors

Affairs Research and Information Management, Kurdistan University of Medical sceinces
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: cesarean section operation under spinal anesthesia, fasting around 6-8 hrs before surgery, Exclusion criteria: gastrointestinal disease, history of middle ear infection and dizziness and moving illness, diabetes and blood pressure illness, smoking and alcohol consumption, using immunosuppressive, fever and infection before surgery, anesthesia and the irregular bleeding long too much, abnormal hemoglobin, receiving any drugs except antibiotics and analgesics up to six hours after surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence and severity of pain, nausia and vometing. Timepoint: Immediately after surgery, 6 hours and 24 hours after surgery. Method of measurement: questionnaire and standard VAS.

Secondary

MeasureTime frame
Incidence and severity of surgery woud infection. Timepoint: 24hours to 14days after cesarean surgery. Method of measurement: ASEPSIS index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJamal Seidy

Kurdestan universty of Medical sciences

jamal.seidy@muk.ac.ir ; jamal.seidi@yahoo.com+98 87 1661 0095

Outcome results

None listed

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