CTRI/2024/03/063927Not yet recruitingUnknown
A randomized controlled double blind trial comparing effect of different pulmonary recruitment manoeuvre pressures on post-laparoscopic shoulder pain - NI
Dr Nithu Dina Joseph0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •ASA I and II patients posted for laparoscopic surgeries under GA of duration upto 4 hours
Exclusion Criteria
- •Patient refusal to participate in study, BMI more than 30, patients with chronic shoulder pain, history of previous shoulder surgery, COPD/respiratory pathologies, patients with hemodynamic instability, high intracranial pressure and right heart failure, pregnancy
Investigators
Similar Trials
Recruiting
Not Applicable
A double blind randomized controlled trial comparing the efficacy of 7% lidocaine / 7% tetracaine cream versus 2,5% lidocaine / 2,5% prilocaine cream for local anaesthesia during laser treatment of acne keloidalis nuchae and tattoo removal.2. acne keloidalis nuchaelaser treatment of: 1. tattoos10040798NL-OMON41973Erasmus MC, Universitair Medisch Centrum Rotterdam30
Active, not recruiting
Not Applicable
A double blind randomized controlled trial comparing the efficacy of two anaesthetic creams for local anaesthesia during laser treatment.Pain during laser treatment of:1. Tattoo 2. Acne keloidalis nuchaeEUCTR2014-003610-86-NL
Completed
Not Applicable
A randomised controlled double blind trial comparing thermal balloon endometrial ablation (Cavaterm) and microwave endometrial ablatioUrological and Genital DiseasesMenorrhagiaISRCTN33718483niversity Hospitals of Leicester NHS Trust (UK)220
Completed
Not Applicable
A double blind randomised controlled trial comparing porcine dermal collagen patch saphenoplasty with conventional saphenofemoral ligation to prevent recurrent saphenofemoral incompetenceISRCTN17706253Record Provided by the NHSTCT Register - 2007 Update - Department of Health80
Completed
Phase 3
A double-blind randomized controlled trial comparing 0.75mg of Palonosetron with 1mg of Granisetron for the control of highly emetogenic chemotherapy-induced emesis.Malignant tumor (lung cancer,gastric cancer,esophagus cancer,cervical cancer,endometrial cancer,head and neck cancer,etc)JPRN-UMIN000004863Pharma Valley Center,Shizuoka Organization for Creation Industries840
