Chlorhexidine Versus Normal Saline Socket Irrigation for Prevention of Dry Socket After Lower Wisdom Tooth Extraction
Comparison of the Effect of Immediate Post-Extraction Socket Irrigation With Normal Saline Versus Chlorhexidine on the Frequency of Dry Socket: A Single-Blinded Randomized Controlled Trial
1 other identifier
interventional
174
1 country
1
Brief Summary
Dry socket, also called alveolar osteitis, is a painful complication that can occur after tooth extraction, particularly following removal of impacted lower wisdom teeth. It occurs when the blood clot that normally forms in the extraction socket is lost or breaks down, resulting in pain and delayed healing. This study will compare two solutions used to irrigate the extraction socket immediately after removal of an impacted lower wisdom tooth: normal saline and chlorhexidine. The study will determine whether immediate socket irrigation with chlorhexidine reduces the frequency of dry socket compared with normal saline. A total of 174 eligible patients undergoing surgical extraction of impacted lower wisdom teeth will be randomly assigned to receive either normal saline or chlorhexidine for immediate post-extraction socket irrigation. Participants will not be informed which irrigation solution they receive. The extraction will be performed by a single surgeon, and postoperative assessment will be performed by a co-researcher. Participants will be assessed for signs and symptoms of dry socket on postoperative days 2, 3, and 5. The occurrence of dry socket will be determined using predefined clinical criteria, including pain, trismus, halitosis, gingival inflammation, exposed or bare bone, radiating pain, and ipsilateral lymphadenopathy. The study will compare the frequency of dry socket between the chlorhexidine and normal saline groups. The findings may help determine whether chlorhexidine is more effective than normal saline for reducing the occurrence of dry socket after surgical extraction of impacted lower wisdom teeth.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 14, 2026
CompletedFirst Submitted
Initial submission to the registry
September 5, 2026
CompletedFirst Posted
Study publicly available on registry
September 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 4, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 28, 2026
ExpectedSeptember 14, 2026
September 1, 2026
8 months
September 5, 2026
September 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frequency of Alveolar Osteitis (Dry Socket)
The frequency of alveolar osteitis (dry socket) will be assessed in participants following surgical extraction of an impacted lower third molar. Alveolar osteitis will be diagnosed when at least three predefined clinical criteria are present, including mild to severe postoperative pain, trismus, halitosis, inflamed or hyperaemic gingiva, exposed or bare bone with an empty socket, radiating pain to the ear or temporal region, and ipsilateral lymphadenopathy. The number and percentage of participants developing alveolar osteitis will be compared between the chlorhexidine and normal saline groups.
Postoperative days 2, 3, and 5
Secondary Outcomes (2)
Postoperative Pain Intensity
Postoperative days 2, 3, and 5
Postoperative Trismus
Postoperative days 2, 3, and 5
Study Arms (2)
Chlorhexidine Socket Irrigation
EXPERIMENTALParticipants allocated to the experimental group will undergo surgical extraction of an impacted lower third molar under local anaesthesia. Immediately after extraction, the extraction socket will be irrigated with chlorhexidine according to the study protocol, followed by socket closure with silk suture. Participants will receive the same postoperative instructions and medications as the comparator group. Postoperative assessment for alveolar osteitis will be performed on days 2, 3, and 5.
Normal Saline Socket Irrigation
ACTIVE COMPARATORParticipants allocated to the comparator group will undergo surgical extraction of an impacted lower third molar under local anaesthesia. Immediately after extraction, the extraction socket will be irrigated with normal saline according to the study protocol, followed by socket closure with silk suture. Participants will receive the same postoperative instructions and medications as the experimental group. Postoperative assessment for alveolar osteitis will be performed on days 2, 3, and 5.
Interventions
Immediate post-extraction irrigation of the surgical extraction socket with chlorhexidine following removal of an impacted lower third molar. The allocated chlorhexidine solution will be applied immediately after extraction and before socket closure with silk suture. The extraction will be performed under local anaesthesia by a single surgeon. The concentration and volume of chlorhexidine will be administered according to the study protocol.
Immediate post-extraction irrigation of the surgical extraction socket with normal saline following removal of an impacted lower third molar. The allocated normal saline solution will be applied immediately after extraction and before socket closure with silk suture. The extraction will be performed under local anaesthesia by a single surgeon. The volume of normal saline will be administered according to the study protocol.
Eligibility Criteria
You may qualify if:
- Adults aged 18 to 50 years.
- Patients requiring surgical extraction of an impacted lower third molar (lower wisdom tooth).
- Impacted lower third molars classified as having slight to moderate difficulty according to Pederson's scale.
- Patients classified as American Society of Anesthesiologists (ASA) physical status I or II.
- Patients of either biological sex.
- Patients who provide written informed consent to participate in the study.
You may not qualify if:
- Systolic blood pressure ≥160 mmHg.
- Diastolic blood pressure ≥100 mmHg.
- Current smokers.
- Alcohol use.
- Patients with muscular diseases.
- Patients currently taking antibiotics or anti-inflammatory medications.
- Patients with physical or mental disabilities that would prevent participation in the study or completion of follow-up assessments.
- Patients requiring extraction without bony osteotomy.
- Deep or very difficult impactions according to Pederson's scale.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CMH Lahore
Lahore, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Asad A Chatha, BDS, FCPS
CMH Lahore Medical College and Institute of Dentistry
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- Participants will be unaware of their assigned socket irrigation solution. The outcome assessor will also be blinded to group allocation during postoperative assessment.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2026
First Posted
September 11, 2026
Study Start
February 14, 2026
Primary Completion
October 4, 2026
Study Completion (Estimated)
October 28, 2026
Last Updated
September 14, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share