An interventional study of Laser therapy and zinc oxide eugenol dressing. in Alveolar Osteitis, sponsored by Badr University. Completed at 1 site in Egypt. Open to female participants aged 25 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-03-10.
Sponsored by Badr University · Not applicable, Interventional, and Treatment
does laser effect on alveolar osteitis recovery in oral contraceptive users ?
photo biomodulation therapy for alveolar osteitis recovery in oral contraceptive users
46 studies on the registry are indexed under Dry Socket; 10 are open to participants now.
This study's enrollment of 50 is below the median of 60 across 41 interventional studies indexed under Dry Socket.
Browse Dry Socket studies →Badr University is the lead sponsor of 64 studies on the registry; 18 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Female patients aged 25-40 years. Currently using oral for at least 3 months prior to participation.
Diagnosed with dry socket (alveolar osteitis) based on clinical criteria.
Presence of systemic diseases (e.g., diabetes, immunodeficiency disorders). Smoking or tobacco use. Allergies to zinc oxide or other study materials. Use of antibiotics or anti-inflammatory medications within the last 2 weeks. Pregnancy or breastfeeding.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Contraception
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
* Laser therapy was administered using a low-level laser device with the following parameters: \[ wavelength 980 nm810, power 500mw, and duration 90 seconds (30second for each 3 sides\]. * Zinc oxide eugenol dressing was applied immediately before the laser therapy. * The intervention will be performed at \[specified intervals every day 0, day7, day 14, day 30)\]
Device: Laser therapy · Device: zinc oxide eugenol dressing.
zinc oxide eugenol dressing.
Device: zinc oxide eugenol dressing.
Laser therapy was administered using a low-level laser device with the following parameters: \[ wavelength 980 nm810, power 500mw, and duration 90 seconds (30second for each 3 sides\].
zinc oxide eugenol dressing.
pain intensity by VAS
Pain intensity measured using a Visual Analog Scale (VAS) at day0, day7, day14 post-treatment.
Time frame: 4 weeks
Socket volume .
measured using \[specific measurement technique, volumetric analysis\] at day0, day14 and 1-month post-treatment
Time frame: 4 weeks
Quality of life assessed
Quality of life assessed using the Oral Health Impact Profile (OHIP-5) questionnaire at day0, day7and day14 post-treatment.
Time frame: 4 weeks
Ran from Nov 2023 to primary completion in Nov 2024, 12 months.
Of 22 interventional studies with no phase under Dry Socket, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 24. This study's 12 months is above that.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Badr University